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Diseases
Genes (528)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
PYGM
Glycogen Storage Disease V
GAMT
Guanidinoacetate Methyltransferase Deficiency
FAM20A
Polyuria
Enamel-Renal Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
MC2R
Familial Glucocorticoid Deficiency
ASS1
Citrullinemia Type I
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
PRKAR1A
Alopecia, Androgenetic, 1
Enamel-Renal Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
AVP
Polyuria
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
Epidermoid Cysts
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
Vascular Tumor