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Diseases
Genes (1138)
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MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
Phyllodes Tumor
PMM2
Pmm2 Deficiency
Muscular Dystrophy
Cutis Laxa
ASL
Argininosuccinic Aciduria
FOXP3
Ipex Syndrome
Phyllodes Tumor
TTPA
Familial Isolated Vitamin E Deficiency
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
TBX5
Holt–oram Syndrome
BLM
Bloom Syndrome
LMNA
Muscular Dystrophy
Emery–dreifuss Muscular Dystrophy
Holt–oram Syndrome
OPA3
Costeff Syndrome
SYNE1
Muscular Dystrophy
Emery–dreifuss Muscular Dystrophy
UMOD
Medullary Cystic Kidney Disease
PQBP1
Renpenning's Syndrome
FBLN5
Cutis Laxa
ELN
Cutis Laxa
DMPK
Myotonic Dystrophy
Muscular Dystrophy
Costeff Syndrome
EFEMP2
Muscular Dystrophy
Cutis Laxa
PYCR1
Cutis Laxa
SYNE2
Muscular Dystrophy
Emery–dreifuss Muscular Dystrophy
LTBP4
Muscular Dystrophy
Cutis Laxa
Bloom Syndrome