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Diseases
Genes (661)
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ATRX
Alpha-Thalassemia Mental Retardation Syndrome
SLC12A6
Andermann Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
PABPN1
Oculopharyngeal Muscular Dystrophy
MED12
Alpha-Thalassemia Mental Retardation Syndrome
Fg Syndrome
TAF1
Dystonia 3, Torsion, X-Linked
UMOD
Medullary Cystic Kidney Disease
SLC20A2
Primary Familial Brain Calcification
PQBP1
Renpenning's Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
DBH
Dopamine Beta Hydroxylase Deficiency
IFIH1
Singleton Merten Syndrome
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
TRNK
Merrf Syndrome