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Diseases
Genes (468)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
CTSD
Harlequin Ichthyosis
Cln10 Disease
ABCA12
Harlequin Ichthyosis
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
GDAP1
Charcot-Marie-Tooth Disease Type 4a
MC2R
Familial Glucocorticoid Deficiency
CA5A
Hyperammonemic Encephalopathy Due To Carbonic Anhydrase Va Deficiency
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
Alopecia, Congenital
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
CILP
Lumbar Disc Disease