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Diseases
Genes (909)
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TTPA
Familial Isolated Vitamin E Deficiency
TBX5
Heart-Hand Syndromes
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
MYH7
Myopathy, Distal, 1
SHH
Holoprosencephaly
SIX3
Holoprosencephaly
TGIF1
Holoprosencephaly
GLI2
Holoprosencephaly
ACTG2
Bronchopulmonary Dysplasia
Berdon Syndrome
NRAS
Neurocutaneous Melanosis
NODAL
Holoprosencephaly
MYH11
Berdon Syndrome
TNF
Bronchopulmonary Dysplasia
Rheumatism
Familial Isolated Vitamin E Deficiency
Listeria Infection
MYLK
Berdon Syndrome
ZIC2
Holoprosencephaly
CDON
Holoprosencephaly
PTCH1
Holoprosencephaly
FGF8
Holoprosencephaly
IL1B
Bronchopulmonary Dysplasia
Rheumatism