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Diseases
Genes (499)
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ABHD5
Cerebral Creatine Deficiency
EFHC1
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
GJA1
Oculodentodigital Dysplasia
MYO5B
Microvillus Inclusion Disease
F12
Factor Xii Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
TMC6
Epidermodysplasia Verruciformis
MC2R
Familial Glucocorticoid Deficiency
GABRA1
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
TMC8
Epidermodysplasia Verruciformis
STX3
Microvillus Inclusion Disease
CACNB4
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
JRK
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
SRD5A2
Alopecia, Androgenetic, 1
TRNK
Merrf Syndrome
AR
Alopecia, Androgenetic, 1