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Diseases
Genes (303)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
TMC6
Epidermodysplasia Verruciformis
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
AGGF1
Klippel-Trenaunay-Weber Syndrome
TMC8
Epidermodysplasia Verruciformis
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
MRAP
Familial Glucocorticoid Deficiency
FH
Fumarase Deficiency
RHOH
Epidermodysplasia Verruciformis
ABCC2
Alopecia, Androgenetic, 1
SUPV3L1
Alopecia, Androgenetic, 1
VDR
Alopecia, Androgenetic, 1
ZFP36
Alopecia, Androgenetic, 1
MTHFR
Alopecia, Androgenetic, 1
TNFRSF10A
Alopecia, Androgenetic, 1