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Diseases
Genes (599)
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TTPA
Familial Isolated Vitamin E Deficiency
MYH7
Laing Early-Onset Distal Myopathy
Familial Isolated Restrictive Cardiomyopathy
RET
Potter Sequence
PQBP1
Renpenning's Syndrome
TNNI3
Familial Isolated Restrictive Cardiomyopathy
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Cystic Hygroma
DICER1
Pinealoblastoma
Dicer1 Syndrome
NEK9
Nevus Comedonicus
IFIH1
Singleton Merten Syndrome
ITGA8
Potter Sequence
AGGF1
Klippel-Trenaunay-Weber Syndrome
PDGFB
Primary Familial Brain Calcification
MTHFR
Spina Bifida
Familial Isolated Vitamin E Deficiency
PAX3
Spina Bifida
GREB1L
Potter Sequence
FREM1
Potter Sequence
FGF20
Potter Sequence
FGFR2
Potter Sequence
Spina Bifida
RB1
Pinealoblastoma
Trilateral Retinoblastoma