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Diseases
Genes (730)
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MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
Phyllodes Tumor
ASL
Argininosuccinic Aciduria
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
FOXP3
Ipex Syndrome
Phyllodes Tumor
TTPA
Familial Isolated Vitamin E Deficiency
COL6A1
Bethlem Myopathy
F12
Factor Xii Deficiency
PMM2
Pmm2 Deficiency
FLNA
Fg Syndrome
Emery–dreifuss Muscular Dystrophy
Phyllodes Tumor
Intestinal Neuronal Dysplasia
ABCC9
Cantú Syndrome
Hippocampal Sclerosis
PQBP1
Renpenning's Syndrome
COL6A3
Bethlem Myopathy
TAF1
Dystonia 3, Torsion, X-Linked
PRPS1
Arts Syndrome
COL6A2
Bethlem Myopathy
UMOD
Medullary Cystic Kidney Disease
SYNE1
Emery–dreifuss Muscular Dystrophy
UBE3B
Kaufman Oculocerebrofacial Syndrome
UBA1
X-Linked Spinal Muscular Atrophy Type 2
LMNA
Emery–dreifuss Muscular Dystrophy
Bethlem Myopathy