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Diseases
Genes (919)
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ABHD5
Cerebral Creatine Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
GNAQ
Sturge–weber Syndrome
RHBDF2
Howel–evans Syndrome
TBX4
Ischiopatellar Dysplasia
MTHFR
Cerebral Softening
Alopecia, Androgenetic, 1
Antiphospholipid Syndrome
Bronchopulmonary Dysplasia
Myelopathy
RASA1
Sturge–weber Syndrome
GLRB
Hyperekplexia
SLC6A5
Hyperekplexia
SRD5A2
Alopecia, Androgenetic, 1
IL1B
Alopecia, Androgenetic, 1
Antiphospholipid Syndrome
Bronchopulmonary Dysplasia
Hippocampal Sclerosis
AR
Alopecia, Androgenetic, 1
FAM155A
Diverticulitis
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
APOH
Antiphospholipid Syndrome
GLRA1
Hyperekplexia
IL10
Hereditary Mucoepithelial Dysplasia
Bronchopulmonary Dysplasia
Chronic Bacterial Prostatitis
Hippocampal Sclerosis
Myelopathy
VDR
Alopecia, Androgenetic, 1
Bronchopulmonary Dysplasia
Myelopathy
PPARG
Antiphospholipid Syndrome
Bronchopulmonary Dysplasia