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Diseases
Genes (933)
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WRN
Werner Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
DKC1
Werner Syndrome
Dyskeratosis Congenita
DMD
Intrauterine Growth Restriction
Duchenne And Becker Muscular Dystrophy
TINF2
Dyskeratosis Congenita
PABPN1
Oculopharyngeal Muscular Dystrophy
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
GLI2
Holoprosencephaly
Medullary Cystic Kidney Disease
SHH
Holoprosencephaly
SIX3
Holoprosencephaly
TGIF1
Holoprosencephaly
ACTG2
Berdon Syndrome
CFH
Pleural Effusion
Membranoproliferative Glomerulonephritis
IFIH1
Singleton Merten Syndrome
TERC
Dyskeratosis Congenita
RTEL1
Dyskeratosis Congenita