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Diseases
Genes (635)
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FMR1
Fragile X Syndrome
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Disinhibition
ASL
Argininosuccinic Aciduria
Hyperoxia
TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
MYO5B
Microvillus Inclusion Disease
PMM2
Pmm2 Deficiency
MED12
Fragile X Syndrome
Fg Syndrome
SLC17A5
Salla Disease
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
STX3
Microvillus Inclusion Disease
MMP2
Avascular Necrosis
Hyperoxia
Lumbar Disc Disease
CYP1A1
Hyperoxia
APP
Fragile X Syndrome
Salla Disease
Disinhibition
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
FOXI1
Enlarged Vestibular Aqueduct
KCNJ10
Enlarged Vestibular Aqueduct
SLC26A4
Enlarged Vestibular Aqueduct
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma