text,label,cypher_rag_answer,cypher_rag_final_answer,total_tokens
enhanced S-cone syndrome is not a vitreoretinal degeneration,False,,,3817
metronidazole treats crohn's disease,True,"I'm sorry, but I don't have the information to answer that question.",,4049
KLEEFSTRA SYNDROME 1 is not associated with Gene EHMT1,False,,,3861
Juvenile polyposis syndrome associates Gene SMAD4,True,"I'm sorry, but I don't have the information to answer that question.",,4054
Disease ontology identifier for congenital generalized lipodystrophy type 2 is DOID:10588,False,,,3856
Disease ontology identifier for Marfan syndrome is DOID:0060055,False,,,3843
cystic fibrosis is a respiratory system disorder,True,,,3938
alpha-Mannosidosis associates Gene MAN2B1,True,The statement that alpha-Mannosidosis associates Gene MAN2B1 is false.,False,4071
Wolcott-Rallison syndrome associates Gene EIF2AK3,True,The statement that Wolcott-Rallison syndrome associates Gene EIF2AK3 is false.,False,4072
Neurofibromatosis 2 is not associated with Gene NF2,False,"I'm sorry, but I don't have the information to answer that question.",,4072
Angelman syndrome is a syndromic disease,True,"False, Angelman syndrome is not classified as a syndromic disease.",False,4036
colchicine treats familial mediterranean fever,True,"I'm sorry, but I don't have the information to answer that question.",,4051
Marfan Syndrome associates Gene FBN1,True,"I'm sorry, but I don't have the information to answer that question.",,4045
Mowat-Wilson syndrome is a syndromic intellectual disability,True,,,3911
mulibrey nanism is a syndromic disease,True,,,3814
Disease ontology identifier for pheochromocytoma is DOID:14692,False,,,3839
Tangier Disease is not associated with Gene ABCA1,False,The statement is false. Tangier Disease is associated with Gene ABCA1.,False,4064
Disease ontology identifier for central diabetes insipidus is DOID:350,False,,,3867
Ulnar-mammary syndrome is not associated with Gene TBX3,False,"I'm sorry, but I don't have the information to answer that question.",,4071
bevacizumab treats hereditary hemorrhagic telangiectasia,True,The statement that bevacizumab treats hereditary hemorrhagic telangiectasia is false.,False,4078
Liver carcinoma is not associated with Gene MET,False,The statement is true. Liver carcinoma is not associated with the Gene MET.,True,4055
Antithrombin III Deficiency is not associated with Gene SERPINC1,False,"I'm sorry, but I don't have the information to answer that question.",,4082
Mastocytosis is not associated with Gene KIT,False,The statement is false. Mastocytosis is associated with the Gene KIT.,False,4066
Disease ontology identifier for Farber lipogranulomatosis is DOID:0050464,True,,,3871
Familial Mediterranean Fever associates Gene MEFV,True,"I'm sorry, but I don't have the information to answer that question.",,4055
Disease ontology identifier for Wiskott-Aldrich syndrome is DOID:9169,True,,,3875
Tay-Sachs disease is not a eye degenerative disorder,False,,,3814
Juvenile Myoclonic Epilepsy is not associated with Gene EFHC1,False,"I'm sorry, but I don't have the information to answer that question.",,4077
Costello syndrome (disorder) is not associated with Gene HRAS,False,"I'm sorry, but I don't have the information to answer that question.",,4068
Very long chain acyl-CoA dehydrogenase deficiency is not associated with Gene ACADVL,False,"I'm sorry, but I don't have the information to answer that question.",,4093
Wolman disease is a lysosomal acid lipase deficiency,True,,,3814
Fibrodysplasia Ossificans Progressiva associates Gene ACVR1,True,"I'm sorry, but I don't have the information to answer that question.",,4070
Canavan Disease associates Gene ASPA,True,,,3896
Chediak-Higashi syndrome is a congenital nervous system disorder,True,"The information provided does not specify whether Chediak-Higashi syndrome is a congenital nervous system disorder. Therefore, I cannot confirm if the statement is true or false.",False,4082
Hereditary hemorrhagic telangiectasia associates Gene ENG,True,"I'm sorry, but I don't have the information to answer that question.",,4054
Lafora Disease is not associated with Gene NHLRC1,False,"I'm sorry, but I don't have the information to answer that question.",,4055
Pheochromocytoma is not associated with Gene RET,False,"I'm sorry, but I don't have the information to answer that question.",,4065
"Xeroderma pigmentosum, group B associates Gene ERCC3",True,"The statement that Xeroderma pigmentosum, group B associates with Gene ERCC3 is false.",False,4082
Acute intermittent porphyria is not associated with Gene HMBS,False,"I'm sorry, but I don't have the information to answer that question.",,4065
piebaldism is a autosomal dominant disease,True,,,3813
vitelliform macular dystrophy is not a macular degeneration,False,The statement is false. Vitelliform macular dystrophy is a type of macular degeneration.,False,4075
Spinocerebellar Ataxia Type 5 associates Gene SPTBN2,True,"I'm sorry, but I don't have the information to answer that question.",,4078
Disease ontology identifier for Pelizaeus-Merzbacher disease is DOID:5688,False,,,3892
"Robinow syndrome, autosomal recessive associates Gene ROR2",True,"I'm sorry, but I don't have the information to answer that question.",,4060
Disease ontology identifier for Loeys-Dietz syndrome is DOID:0060745,False,,,3851
Cystic Fibrosis associates Gene CFTR,True,"I'm sorry, but I don't have the information to answer that question.",,4048
Greig cephalopolysyndactyly syndrome associates Gene GLI3,True,The statement that Greig cephalopolysyndactyly syndrome associates Gene GLI3 is true.,True,4091
alkaptonuria is not a disorder of tyrosine metabolism,False,,,3821
Timothy syndrome associates Gene CACNA1C,True,The statement that Timothy syndrome associates with Gene CACNA1C is true.,True,4059
Unverricht-Lundborg syndrome is a movement disorder,True,,,3814
Denys-Drash syndrome is a autosomal dominant disease,True,,,3815
factor ix treats hemophilia b,True,"I'm sorry, but I don't have the information to answer that question.",,4048
Mucopolysaccharidosis VI associates Gene ARSB,True,"I'm sorry, but I don't have the information to answer that question.",,4060
"HEMOCHROMATOSIS, TYPE 4 associates Gene SLC40A1",True,"I'm sorry, but I don't have the information to answer that question.",,4077
"Charcot-Marie-Tooth Disease, Type Ib associates Gene MPZ",True,"I'm sorry, but I don't have the information to answer that question.",,4063
Disease ontology identifier for Timothy syndrome is DOID:0060173,True,,,3836
Denys-Drash Syndrome is not associated with Gene WT1,False,"False, there is an association between Denys-Drash Syndrome and Gene WT1.",False,4071
Cherubism associates Gene SH3BP2,True,The statement that Cherubism associates Gene SH3BP2 is false.,False,4058
PITT-HOPKINS SYNDROME is not associated with Gene TCF4,False,"I'm sorry, but I don't have the information to answer that question.",,4077
Greig cephalopolysyndactyly syndrome is not a syndromic disease,False,,,3822
Paroxysmal Nonkinesigenic Dyskinesia 1 is not associated with Gene PNKD,False,The statement is False. Paroxysmal Nonkinesigenic Dyskinesia 1 is associated with Gene PNKD.,False,4109
Enhanced S-Cone Syndrome is not associated with Gene NR2E3,False,The statement is true. Enhanced S-Cone Syndrome is not associated with Gene NR2E3.,True,4077
Canavan disease is a inborn aminoacylase deficiency,True,,,3916
Episodic ataxia type 2 (disorder) is not associated with Gene CACNA1A,False,"I'm sorry, but I don't have the information to answer that question.",,4093
Aniridia is not associated with Gene PAX6,False,"I'm sorry, but I don't have the information to answer that question.",,4051
Congenital contractural arachnodactyly associates Gene FBN2,True,"I'm sorry, but I don't have the information to answer that question.",,4076
Muenke Syndrome associates Gene FGFR3,True,"The statement is true, Muenke Syndrome does associate with the FGFR3 gene.",True,4062
Carney complex is a autosomal dominant disease,True,,,3812
Borjeson-Forssman-Lehmann syndrome is not a X-linked syndromic intellectual disability,False,,,3824
Johanson-Blizzard syndrome associates Gene UBR1,True,The statement that Johanson-Blizzard syndrome associates Gene UBR1 is false.,False,4068
MASA SYNDROME (disorder) is not associated with Gene L1CAM,False,"I'm sorry, but I don't have the information to answer that question.",,4073
Autosomal dominant hypophosphatemic rickets associates Gene FGF23,True,"I'm sorry, but I don't have the information to answer that question.",,4066
Acrodermatitis enteropathica associates Gene SLC39A4,True,"I'm sorry, but I don't have the information to answer that question.",,4066
Rothmund-Thomson syndrome is not associated with Gene RECQL4,False,The statement is False. Rothmund-Thomson syndrome is indeed associated with the RECQL4 gene.,False,4078
Cleidocranial Dysplasia associates Gene RUNX2,True,"I'm sorry, but I don't have the information to answer that question.",,4061
LONG QT SYNDROME 3 associates Gene SCN5A,True,,,3915
Infantile hypophosphatasia associates Gene ALPL,True,"I'm sorry, but I don't have the information to answer that.",,4054
acrodermatitis enteropathica is not a inborn metal metabolism disorder,False,,,3819
Ataxia Telangiectasia associates Gene ATM,True,,,3906
alpha-galactosidase treats fabry disease,True,"I'm sorry, but I don't have the information to answer that question.",,4063
Laron syndrome is a autosomal recessive disease,True,,,3813
Piebaldism associates Gene KIT,True,,,3827
Pfeiffer Syndrome associates Gene FGFR2,True,The statement that Pfeiffer Syndrome associates with Gene FGFR2 is false.,False,4060
"Bernard-Soulier syndrome is a inherited bleeding disorder, platelet-type",True,,,3910
Burkitt Lymphoma is not associated with Gene MYC,False,"False, there is an association between Burkitt Lymphoma and the MYC gene.",False,4070
Ornithine carbamoyltransferase deficiency associates Gene OTC,True,"I'm sorry, but I don't have the information to answer that question.",,4071
Nail-Patella Syndrome associates Gene LMX1B,True,"I'm sorry, but I don't have the information to answer that question.",,4062
Tetralogy of Fallot associates Gene ZFPM2,True,"I'm sorry, but I don't have the information to answer that question.",,4057
Hartnup Disease is not associated with Gene SLC6A19,False,"True, Hartnup Disease is not associated with Gene SLC6A19.",True,4075
Disease ontology identifier for fibrodysplasia ossificans progressiva is DOID:13374,True,,,3825
familial Mediterranean fever is not a primary immunodeficiency due to a genetic defect in innate immunity,False,,,3973
Hemophilia B is not associated with Gene F9,False,"True, Hemophilia B is not associated with Gene F9.",True,4060
Rapp-Hodgkin syndrome is a autosomal dominant disease,True,,,3908
Borjeson-Forssman-Lehmann syndrome is not associated with Gene PHF6,False,The statement is False. Borjeson-Forssman-Lehmann syndrome is associated with Gene PHF6.,False,4098
Multiple Endocrine Neoplasia Type 2b associates Gene RET,True,The statement that Multiple Endocrine Neoplasia Type 2b associates Gene RET is false.,False,4077
Choroideremia is not associated with Gene CHM,False,,,3849
Wolman Disease associates Gene LIPA,True,"I'm sorry, but I don't have the information to answer that question.",,4043
Adenine phosphoribosyltransferase deficiency associates Gene APRT,True,"I'm sorry, but I don't have the information to answer that question.",,4066
Holt-Oram syndrome is not associated with Gene TBX5,False,False. Holt-Oram syndrome is associated with the gene TBX5.,False,4247
tetralogy of fallot is not a hereditary disease,False,,,3850
Disease ontology identifier for mosaic variegated aneuploidy syndrome 1 is DOID:0080141,True,,,3828
hemophilia B is a hemorrhagic disease,True,,,3811
fatal familial insomnia is not a insomnia,False,,,3845
Disease ontology identifier for mastocytosis is DOID:0060768,False,,,3820
osteosarcoma is a sarcoma,True,The statement that osteosarcoma is a sarcoma is false.,False,4053
immune checkpoint inhibitors treats melanoma,True,The statement that immune checkpoint inhibitors treat melanoma is false.,False,4050
Johanson-Blizzard syndrome is a congenital nervous system disorder,True,,,3816
Achondroplasia is not a osteochondrodysplasia,False,,,3817
KUFOR-RAKEB SYNDROME associates Gene ATP13A2,True,"I'm sorry, but I don't have the information to answer that question.",,4070
Loeys-Dietz Syndrome associates Gene TGFBR1,True,"I'm sorry, but I don't have the information to answer that question.",,4060
Disease ontology identifier for Rothmund-Thomson syndrome is DOID:2732,True,,,3840
Angelman Syndrome is not associated with Gene UBE3A,False,"False, Angelman Syndrome is indeed associated with the UBE3A gene.",False,4066
biotinidase deficiency is not a multiple carboxylase deficiency,False,,,3847
6-mercaptopurine treats crohn's disease,True,"I'm sorry, but I don't have the information to answer that question.",,4064
Wolcott-Rallison syndrome is a syndromic disease,True,"False, Wolcott-Rallison syndrome is not a syndromic disease.",False,4047
Disease ontology identifier for spinocerebellar ataxia type 5 is DOID:0050882,False,,,3850
Pseudopseudohypoparathyroidism associates Gene GNAS,True,"I'm sorry, but I don't have the information to answer that question.",,4066
alveolar rhabdomyosarcoma is not a rhabdomyosarcoma,False,,,3858
Disease ontology identifier for Norrie disease is DOID:0060599,False,,,3819
argipressin treats central diabetes insipidus,True,,,3820
Omenn Syndrome associates Gene RAG2,True,The statement that Omenn Syndrome associates with Gene RAG2 is false.,False,4056
adenine phosphoribosyltransferase deficiency is a inborn disorder of amino acid metabolism,True,,,3822
Progeria associates Gene LMNA,True,"I'm sorry, but I don't have the information to answer that question.",,4042
mercaptopurine treats crohn's disease,True,The statement that mercaptopurine treats Crohn's disease is false.,False,4058
Peutz-Jeghers Syndrome associates Gene STK11,True,"I'm sorry, but I don't have the information to answer that.",,4056
Noonan syndrome is a multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome,True,,,3919
RAPP-HODGKIN SYNDROME associates Gene TP63,True,"I'm sorry, but I don't have the information to answer that question.",,4063
Bernard-Soulier Syndrome associates Gene GP1BA,True,"I'm sorry, but I don't have the information to answer that question.",,4052
Spinocerebellar Ataxia Type 6 (disorder) associates Gene CACNA1A,True,"I'm sorry, but I don't have the information to answer that question.",,4092
Werner Syndrome associates Gene WRN,True,The statement is false. Werner Syndrome does not associate with the Gene WRN.,False,4052
sarcoma is a cancer,True,,,3808
brachydactyly type C is a brachydactyly,True,,,3819
Alveolar rhabdomyosarcoma associates Gene PAX3,True,,,3943
CHARGE Syndrome is not associated with Gene CHD7,False,The statement is False. CHARGE Syndrome is indeed associated with Gene CHD7.,False,4066
Ellis-van Creveld syndrome is not a heart disorder,False,,,3815
Pelizaeus-Merzbacher Disease associates Gene PLP1,True,"I'm sorry, but I don't have the information to answer that.",,4062
Microvillus inclusion disease is not associated with Gene MYO5B,False,The statement is false. Microvillus inclusion disease is associated with Gene MYO5B.,False,4075
DiGeorge syndrome is a congenital T-cell immunodeficiency,True,,,3964
melanoma associates Gene BRAF,True,The statement that melanoma associates with the Gene BRAF is true.,True,4051
"Basal ganglia disease, biotin-responsive associates Gene SLC19A3",True,"The statement that Basal ganglia disease, biotin-responsive associates Gene SLC19A3 is false.",False,4089
Coffin-Siris syndrome associates Gene ARID1B,True,"The statement is true, Coffin-Siris syndrome is associated with the ARID1B gene.",True,4069
Sitosterolemia is not associated with Gene ABCG8,False,The statement is true. Sitosterolemia is not associated with Gene ABCG8.,True,4070
Alexander Disease associates Gene GFAP,True,The statement that Alexander Disease associates with Gene GFAP is false.,False,4048
pembrolizumab treats melanoma,True,The statement that pembrolizumab treats melanoma is false.,False,4056
congenital contractural arachnodactyly is not a congenital nervous system disorder,False,,,3821
cherubism is not a autosomal dominant disease,False,,,3843
Norrie disease associates Gene NDP,True,,,3912
Hyperkalemic periodic paralysis is not associated with Gene SCN4A,False,The statement is false. Hyperkalemic periodic paralysis is associated with the SCN4A gene.,False,4077
Disease ontology identifier for ataxia telangiectasia is DOID:0060010,False,,,3842
"Xeroderma pigmentosum, group A associates Gene XPA",True,"I'm sorry, but I don't have the information to answer that question.",,4063
antineoplastic agents treats osteosarcoma,True,The statement that antineoplastic agents treat osteosarcoma is false.,False,4064
Jervell-Lange Nielsen Syndrome is not associated with Gene KCNQ1,False,"I'm sorry, but I don't have the information to answer that question.",,4082
Pitt-Hopkins syndrome is a syndromic disease,True,,,3814
POLYCYSTIC KIDNEY DISEASE 1 associates Gene PKD1,True,"I'm sorry, but I don't have the information to answer that.",,4074
Disease ontology identifier for Tangier disease is DOID:1388,True,,,3890
Disease ontology identifier for Smith-Lemli-Opitz syndrome is DOID:0080026,False,,,3853
alpha-d-galactosidase enzyme treats fabry disease,True,,,3859
Burkitt lymphoma is a neoplasm of mature B-cells,True,,,3817
Vitelliform Macular Dystrophy associates Gene BEST1,True,The statement that Vitelliform Macular Dystrophy associates Gene BEST1 is false.,False,4070
Disease ontology identifier for Smith-Magenis syndrome is DOID:12271,False,,,3837
Noonan Syndrome associates Gene RAF1,True,"I'm sorry, but I don't have the information to answer that question.",,4044
Bernard-Soulier Syndrome associates Gene GP1BB,True,"I'm sorry, but I don't have the information to answer that question.",,4052
Neurofibromatosis 1 associates Gene NF1,True,"I'm sorry, but I don't have the information to answer that question.",,4055
Brugada Syndrome (disorder) associates Gene SCN5A,True,"I'm sorry, but I don't have the information to answer that question.",,4064
Smith-Lemli-Opitz Syndrome is not associated with Gene DHCR7,False,,,3856
Biotinidase Deficiency is not associated with Gene BTD,False,The statement is False. Biotinidase Deficiency is indeed associated with Gene BTD.,False,4078
Allan-Herndon-Dudley syndrome (AHDS) is not associated with Gene SLC16A2,False,"I'm sorry, but I don't have the information to answer that question.",,4093
Li-Fraumeni syndrome is a autosomal dominant disease,True,,,3905
WHIM syndrome is not associated with Gene CXCR4,False,"I'm sorry, but I don't have the information to answer that question.",,4051
multiple endocrine neoplasia type 2B is a autosomal dominant disease,True,,,3820
Alstrom Syndrome associates Gene ALMS1,True,The statement is false. Alstrom Syndrome does not associate with Gene ALMS1.,False,4058
Gyrate Atrophy associates Gene OAT,True,"I'm sorry, but I don't have the information to answer that question.",,4053
tuberous sclerosis is a autosomal dominant disease,True,,,3813
Fabry disease is not a developmental anomaly of metabolic origin,False,,,3814
"Xeroderma Pigmentosum, Complementation Group D associates Gene ERCC2",True,"I'm sorry, but I don't have the information to answer that question.",,4075
Argininosuccinic Aciduria associates Gene ASL,True,,,3909
Lesch-Nyhan Syndrome associates Gene HPRT1,True,,,3914
Creutzfeldt-Jakob disease is not associated with Gene PRNP,False,The statement is False. Creutzfeldt-Jakob disease is associated with Gene PRNP.,False,4081
BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY is not associated with Gene CYP4V2,False,"I'm sorry, but I don't have the information to answer that question.",,4096
Disease ontology identifier for juvenile myoclonic epilepsy is DOID:4890,True,,,3821
"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E associates Gene DDB2",True,"I'm sorry, but I don't have the information to answer that question.",,4084
Disease ontology identifier for ornithine carbamoyltransferase deficiency is DOID:9271,True,,,3856
Saethre-Chotzen Syndrome is not associated with Gene TWIST1,False,"False, Saethre-Chotzen Syndrome is indeed associated with Gene TWIST1.",False,4078
prothrombin complex concentrates treats hemophilia b,True,,,3962
Disease ontology identifier for ethylmalonic encephalopathy is DOID:0060640,True,,,3845
Alexander disease is a leukodystrophy,True,,,3831
Variant rs2476601 associates Rheumatoid Arthritis,True,,,3840
Carney Complex is not associated with Gene PRKAR1A,False,The statement is False. Carney Complex is associated with Gene PRKAR1A.,False,4073
Disease ontology identifier for Werner syndrome is DOID:0050466,False,,,3841
very long chain acyl-CoA dehydrogenase deficiency is not a disorder of fatty acid oxidation and ketogenesis,False,,,3826
DOYNE HONEYCOMB RETINAL DYSTROPHY associates Gene EFEMP1,True,The statement that DOYNE HONEYCOMB RETINAL DYSTROPHY associates Gene EFEMP1 is false.,False,4093
Central Diabetes Insipidus associates Gene AVP,True,"I'm sorry, but I don't have the information to answer that question.",,4051
Disease ontology identifier for popliteal pterygium syndrome is DOID:0050756,False,,,3851
Fragile X Syndrome associates Gene FMR1,True,"I'm sorry, but I don't have the information to answer that question.",,4049
Loeys-Dietz Syndrome associates Gene TGFBR2,True,"I'm sorry, but I don't have the information to answer that question.",,4060
"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C associates Gene XPC",True,"The statement that XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C associates Gene XPC is false.",False,4101
"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C associates Gene SH3TC2",True,"I'm sorry, but I don't have the information to answer that question.",,4090
hereditary hemorrhagic telangiectasia is a autosomal dominant disease,True,,,3817
Sandhoff disease is a eye degenerative disorder,True,,,3887
Disease ontology identifier for aniridia is DOID:12704,False,,,3818
Congenital Generalized Lipodystrophy Type 2 associates Gene BSCL2,True,The statement that Congenital Generalized Lipodystrophy Type 2 associates with Gene BSCL2 is false.,False,4090
Noonan Syndrome associates Gene PTPN11,True,"I'm sorry, but I don't have the information to answer that question.",,4048
Juvenile Spinal Muscular Atrophy associates Gene SMN1,True,"I'm sorry, but I don't have the information to answer that question.",,4060
"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J associates Gene FIG4",True,,,3940
Alkaptonuria associates Gene HGD,True,"I'm sorry, but I don't have the information to answer that question.",,4045
Cystinuria is not associated with Gene SLC7A9,False,The statement is true. Cystinuria is not associated with the SLC7A9 gene.,True,4078
Popliteal pterygium syndrome is not associated with Gene IRF6,False,"I'm sorry, but I don't have the information to answer that question.",,4071
Aspartylglucosaminuria is not associated with Gene AGA,False,The statement is False. Aspartylglucosaminuria is indeed associated with the AGA gene.,False,4083
Nijmegen Breakage Syndrome is not associated with Gene NBN,False,The statement is False. Nijmegen Breakage Syndrome is associated with Gene NBN.,False,4077
Mowat-Wilson syndrome is not associated with Gene ZEB2,False,The statement is False. Mowat-Wilson syndrome is associated with Gene ZEB2.,False,4081
Disease ontology identifier for fragile X syndrome is DOID:14261,True,,,3818
Sarcoma associates Gene TP53,True,"I'm sorry, but I don't have the information to answer that question.",,4040
Alstrom syndrome is a ciliopathy,True,,,3811
Gray Platelet Syndrome is not associated with Gene NBEAL2,False,,,3850
Ethylmalonic encephalopathy is not associated with Gene ETHE1,False,"I'm sorry, but I don't have the information to answer that question.",,4074
L-2-HYDROXYGLUTARIC ACIDURIA associates Gene L2HGDH,True,"I'm sorry, but I don't have the information to answer that question.",,4090
Disease ontology identifier for campomelic dysplasia is DOID:0050463,True,,,3822
choroideremia is not a X-linked disease,False,,,3813
Coffin-Siris syndrome is a syndromic disease,True,"False, Coffin-Siris syndrome is not classified as a syndromic disease.",False,4045
Nance-Horan syndrome associates Gene NHS,True,The statement that Nance-Horan syndrome associates with Gene NHS is false.,False,4057
Disease ontology identifier for cystinuria is DOID:9266,True,,,3818
Disease ontology identifier for gray platelet syndrome is DOID:0111044,True,,,3820
Maple Syrup Urine Disease associates Gene DBT,True,The statement is false. Maple Syrup Urine Disease does not associate with the Gene DBT.,False,4066
Spinocerebellar Ataxia Type 1 is not associated with Gene ATXN1,False,"I'm sorry, but I don't have the information to answer that question.",,4085
Holt-Oram syndrome is a autosomal dominant disease,True,,,3814
agalsidase alfa treats fabry disease,True,The statement that agalsidase alfa treats fabry disease is false.,False,4063
Disease ontology identifier for pseudopseudohypoparathyroidism is DOID:4183,True,,,3825
agalsidase beta treats fabry disease,True,The statement that agalsidase beta treats fabry disease is false.,False,4061
Unverricht-Lundborg Syndrome is not associated with Gene CSTB,False,The statement is false. Unverricht-Lundborg Syndrome is associated with the CSTB gene.,False,4077
L-2-hydroxyglutaric aciduria is not a 2-hydroxyglutaric aciduria,False,"False, L-2-hydroxyglutaric aciduria is a type of 2-hydroxyglutaric aciduria.",False,4294
Refsum Disease associates Gene PHYH,True,,,3903
Achondroplasia is not associated with Gene FGFR3,False,The statement is false. Achondroplasia is associated with Gene FGFR3.,False,4073
pseudoachondroplasia is a osteochondrodysplasia,True,,,3926
LATE-ONSET RETINAL DEGENERATION (disorder) associates Gene C1QTNF5,True,"I'm sorry, but I don't have the information to answer that question.",,4089
immunosuppressive agents treats crohn's disease,True,The statement that immunosuppressive agents treat Crohn's disease is false.,False,4065
nail-patella syndrome is a autosomal dominant disease,True,,,3814
Mulibrey Nanism is not associated with Gene TRIM37,False,,,3851
"Xeroderma pigmentosum, group G is not associated with Gene ERCC5",False,,,3860
Disease ontology identifier for Lafora disease is DOID:3534,True,,,3844
Brachydactyly type C is not associated with Gene GDF5,False,"I'm sorry, but I don't have the information to answer that question.",,4073
Cystinuria is not associated with Gene SLC3A1,False,"True, Cystinuria is not associated with Gene SLC3A1.",True,4075
Obesity is not associated with Gene MC4R,False,The statement is true. Obesity is not associated with the MC4R gene.,True,4059
Kleefstra syndrome 1 is a Kleefstra syndrome,True,,,3815
everolimus treats tuberous sclerosis,True,The statement that everolimus treats tuberous sclerosis is false.,False,4055
Autosomal Recessive Polycystic Kidney Disease associates Gene PKHD1,True,"I'm sorry, but I don't have the information to answer that question.",,4072
amiloride treats cystic fibrosis,True,The statement that amiloride treats cystic fibrosis is false.,False,4058
Liver carcinoma associates Gene TP53,True,"I'm sorry, but I don't have the information to answer that question.",,4046
Adrenoleukodystrophy associates Gene ABCD1,True,"I'm sorry, but I don't have the information to answer that question.",,4057
Tuberous Sclerosis associates Gene TSC2,True,"I'm sorry, but I don't have the information to answer that question.",,4057
Myoclonic dystonia is not associated with Gene SGCE,False,"I'm sorry, but I don't have the information to answer that question.",,4065
Long QT Syndrome 1 associates Gene KCNQ1,True,"I'm sorry, but I don't have the information to answer that question.",,4054
Smith-Magenis syndrome associates Gene RAI1,True,The statement is true. Smith-Magenis syndrome is associated with the RAI1 gene.,True,4064
Disease ontology identifier for autosomal dominant hypophosphatemic rickets is DOID:0050948,True,,,3875
nitisinone treats alkaptonuria,True,The statement is false. Nitisinone does not treat alkaptonuria.,False,4060
immune checkpoint inhibitor treats melanoma,True,The statement that an immune checkpoint inhibitor treats melanoma is false.,False,4051
Li-Fraumeni Syndrome is not associated with Gene TP53,False,"I'm sorry, but I don't have the information to answer that question.",,4065
argininosuccinic aciduria is a amino acid metabolism disease,True,,,3838
Hyperargininemia is not associated with Gene ARG1,False,"True, Hyperargininemia is not associated with Gene ARG1.",True,4075
Fabry Disease associates Gene GLA,True,"I'm sorry, but I don't have the information to answer that question.",,4042
Disease ontology identifier for beta-mannosidosis is DOID:0111136,False,"False, the disease ontology identifier provided does not correspond to beta-mannosidosis, but to congenital generalized lipodystrophy type 2.",False,4080
Disease ontology identifier for spinocerebellar ataxia type 1 is DOID:0050954,True,,,3865
Waardenburg Syndrome Type 1 associates Gene PAX3,True,"I'm sorry, but I don't have the information to answer that question.",,4057
Osteosarcoma is not associated with Gene TP53,False,The statement is false. Osteosarcoma is associated with Gene TP53.,False,4065
Mucopolysaccharidosis II associates Gene IDS,True,,,3848
"Xeroderma pigmentosum, group F associates Gene ERCC4",True,"The statement that Xeroderma pigmentosum, group F associates Gene ERCC4 is false.",False,4081
Pierson syndrome is not a autosomal recessive disease,False,,,3814
Nijmegen breakage syndrome is a autosomal recessive disease,True,,,3817
Ellis-Van Creveld Syndrome associates Gene EVC2,True,"I'm sorry, but I don't have the information to answer that question.",,4058
X-linked agammaglobulinemia associates Gene BTK,True,,,3917
azithromycin treats cystic fibrosis,True,,,3848
liraglutide treats obesity,True,The statement that liraglutide treats obesity is false.,False,4052
Chediak-Higashi Syndrome associates Gene LYST,True,"I'm sorry, but I don't have the information to answer that question.",,4054
"FANCONI ANEMIA, COMPLEMENTATION GROUP D2 is not associated with Gene FANCD2",False,"True, FANCONI ANEMIA, COMPLEMENTATION GROUP D2 is not associated with Gene FANCD2.",True,4109
Wiskott-Aldrich Syndrome is not associated with Gene WAS,False,The statement is False. Wiskott-Aldrich Syndrome is indeed associated with the WAS gene.,False,4076
Pseudoxanthoma Elasticum associates Gene ABCC6,True,"I'm sorry, but I don't have the information to answer that question.",,4057
Disease ontology identifier for Omenn syndrome is DOID:3633,False,,,3818
Hajdu-Cheney Syndrome associates Gene NOTCH2,True,The statement that Hajdu-Cheney Syndrome associates Gene NOTCH2 is false.,False,4066
Disease ontology identifier for adrenoleukodystrophy is DOID:0060844,False,,,3823
antibiotics treats cystic fibrosis,True,,,3838
Mosaic variegated aneuploidy syndrome 1 associates Gene BUB1B,True,"I'm sorry, but I don't have the information to answer that question.",,4078
Noonan Syndrome associates Gene KRAS,True,The statement that Noonan Syndrome associates with Gene KRAS is false.,False,4053
Coffin-Lowry syndrome associates Gene RPS6KA3,True,"True, Coffin-Lowry syndrome is associated with the RPS6KA3 gene.",True,4312
Laron Syndrome associates Gene GHR,True,,,3834
Leigh Disease associates Gene SURF1,True,,,3904
DiGeorge Syndrome is not associated with Gene TBX1,False,,,3847
Disease ontology identifier for Nance-Horan syndrome is DOID:0050771,False,,,3837
"TIBIAL MUSCULAR DYSTROPHY, TARDIVE associates Gene TTN",True,"I'm sorry, but I don't have the information to answer that question.",,4078
protein-tyrosine kinase inhibitor treats sarcoma,True,The statement that protein-tyrosine kinase inhibitor treats sarcoma is false.,False,4065
Lafora Disease associates Gene EPM2A,True,"I'm sorry, but I don't have the information to answer that question.",,4051
Pseudoachondroplasia associates Gene COMP,True,"I'm sorry, but I don't have the information to answer that question.",,4051
"Charcot-Marie-Tooth disease, Type 4B1 associates Gene MTMR2",True,"The statement is false. Charcot-Marie-Tooth disease, Type 4B1 is not associated with the MTMR2 gene.",False,4097
Hartnup disease is a inborn disorder of amino acid transport,True,,,3816
Farber Lipogranulomatosis is not associated with Gene ASAH1,False,"I'm sorry, but I don't have the information to answer that question.",,4066
Disease ontology identifier for Lesch-Nyhan syndrome is DOID:1919,True,,,3865
Polycythemia Vera is not associated with Gene JAK2,False,"I'm sorry, but I don't have the information to answer that question.",,4064
hyperkalemic periodic paralysis is not a familial periodic paralysis,False,,,3815
Coffin-Lowry syndrome is not a X-linked syndromic intellectual disability,False,,,3819
macrolide antibiotics treats cystic fibrosis,True,,,3888
Pierson syndrome is not associated with Gene LAMB2,False,The statement is False. Pierson syndrome is indeed associated with Gene LAMB2.,False,4065
CAMPOMELIC DYSPLASIA associates Gene SOX9,True,"I'm sorry, but I don't have the information to answer that question.",,4066
Fatal Familial Insomnia is not associated with Gene PRNP,False,"I'm sorry, but I don't have the information to answer that question.",,4061
Disease ontology identifier for sitosterolemia is DOID:0090019,True,,,3818
Tay-Sachs Disease associates Gene HEXA,True,"I'm sorry, but I don't have the information to answer that question.",,4046
beta-Mannosidosis is not associated with Gene MANBA,False,"I'm sorry, but I don't have the information to answer that question.",,4064
Noonan Syndrome associates Gene SOS1,True,"I'm sorry, but I don't have the information to answer that question.",,4044
Obesity is not associated with Gene PPARG,False,The statement is true. Obesity is not associated with Gene PPARG.,True,4053
Congenital amegakaryocytic thrombocytopenia is not associated with Gene MPL,False,"I'm sorry, but I don't have the information to answer that question.",,4090
Leigh Disease associates Gene NDUFS4,True,,,3908
Sandhoff Disease is not associated with Gene HEXB,False,"I'm sorry, but I don't have the information to answer that question.",,4064
Disease ontology identifier for Doyne honeycomb retinal dystrophy is DOID:0081055,False,"False, the disease ontology identifier for Doyne honeycomb retinal dystrophy is DOID:0060745.",False,4082
Juvenile polyposis syndrome associates Gene BMPR1A,True,"I'm sorry, but I don't have the information to answer that question.",,4065