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Diseases
Genes (908)
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ASL
Argininosuccinic Aciduria
GLDC
Infantile Glycine Encephalopathy
PMM2
Pmm2 Deficiency
MAGEL2
Prader-Willi Syndrome
SNRPN
Prader-Willi Syndrome
AMT
Infantile Glycine Encephalopathy
GCSH
Infantile Glycine Encephalopathy
NDN
Prader-Willi Syndrome
FLG
Dry Skin
Dermatitis
Keratosis Pilaris
KCNAB2
Chromosome 1p36 Deletion Syndrome
NOD2
Dry Skin
Dermatitis
MKRN3
Prader-Willi Syndrome
IL4
Dermatitis
IFNG
Dermatitis
Pontiac Fever
NPAP1
Prader-Willi Syndrome
IPW
Prader-Willi Syndrome
PWAR1
Prader-Willi Syndrome
SHARPIN
Dermatitis
IL13
Dermatitis
SNORD116-1
Prader-Willi Syndrome