Source: CLINVAR

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C1868690
Disease: Hypoadrenocorticism, familial
Hypoadrenocorticism, familial
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0269269
Disease: Inversion of nipple (disorder)
Inversion of nipple (disorder)
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0027059
Disease: Myocarditis
Myocarditis
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0231687
Disease: Spastic gait
Spastic gait
phenotype 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting
phenotype 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0036572
Disease: Seizures
Seizures
phenotype 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C1836830
Disease: Developmental regression
Developmental regression
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
disease 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation
phenotype 0.100 None 0 1
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
ATP binding cassette subfamily D member 1 0.563 0.731 1.00
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
phenotype 0.100 None 0 1