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Diseases
Genes (418)
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GLDC
Infantile Glycine Encephalopathy
MAGEL2
Prader-Willi Syndrome
SLC2A10
Hiatal Hernia
Arterial Tortuosity Syndrome
SNRPN
Prader-Willi Syndrome
AMT
Infantile Glycine Encephalopathy
GCSH
Infantile Glycine Encephalopathy
NDN
Prader-Willi Syndrome
KCNAB2
Chromosome 1p36 Deletion Syndrome
MKRN3
Prader-Willi Syndrome
NPAP1
Prader-Willi Syndrome
IPW
Prader-Willi Syndrome
PWAR1
Prader-Willi Syndrome
ALDH2
Alcohol Intolerance
Macrocytosis
SNORD116-1
Prader-Willi Syndrome
MKRN3-AS1
Prader-Willi Syndrome
SKI
Chromosome 1p36 Deletion Syndrome
PRDM16
Chromosome 1p36 Deletion Syndrome
PWRN1
Prader-Willi Syndrome
SNORD115-1
Prader-Willi Syndrome
RERE
Chromosome 1p36 Deletion Syndrome