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Diseases
Genes (1144)
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ATRX
Adenoid Cystic Carcinoma
Alpha-Thalassemia Mental Retardation Syndrome
MED12
Fg Syndrome
Phyllodes Tumor
Alpha-Thalassemia Mental Retardation Syndrome
FOXP3
Phyllodes Tumor
Ipex Syndrome
Chronic Multifocal Langerhans Cell Histiocytosis
BLM
Bloom Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
TBX5
Holt–oram Syndrome
FMR1
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Rolandic Epilepsy
ABCC9
Cantú Syndrome
Hippocampal Sclerosis
FECH
Erythropoietic Protoporphyria
TP53
Adenoid Cystic Carcinoma
Bloom Syndrome
Gastrinoma
Phyllodes Tumor
Chronic Multifocal Langerhans Cell Histiocytosis
Alpha-Thalassemia Mental Retardation Syndrome
PQBP1
Renpenning's Syndrome
BRAF
Hippocampal Sclerosis
Chronic Multifocal Langerhans Cell Histiocytosis
Vascular Malformation
UMOD
Medullary Cystic Kidney Disease
TAF1
Dystonia 3, Torsion, X-Linked
UBE3B
Kaufman Oculocerebrofacial Syndrome
FBLN5
Cutis Laxa
ELN
Cutis Laxa
KCNJ8
Cantú Syndrome
PYCR1
Cutis Laxa
EFEMP2
Cutis Laxa