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Diseases
Genes (1346)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
SMARCB1
Medulloblastoma
Pinealoblastoma
Schwannomatosis
PTCH1
Medulloblastoma
CTSD
Harlequin Ichthyosis
Cln10 Disease
ABCA12
Harlequin Ichthyosis
CTNNB1
Alopecia, Androgenetic, 1
Medulloblastoma
Harlequin Ichthyosis
SUFU
Medulloblastoma
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GDAP1
Charcot-Marie-Tooth Disease Type 4a
APC
Medulloblastoma
SMO
Medulloblastoma
MC2R
Familial Glucocorticoid Deficiency
CA5A
Hyperammonemic Encephalopathy Due To Carbonic Anhydrase Va Deficiency
IFIH1
Singleton Merten Syndrome
BRD4
Alopecia, Androgenetic, 1
Medulloblastoma
BRCA2
Medulloblastoma
NBN
Medulloblastoma
PTCH2
Medulloblastoma