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Diseases
Genes (740)
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LCAT
Fish-Eye Disease
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
RET
Multiple Endocrine Neoplasia Type 2
MYH7
Laing Distal Myopathy
ANKRD26
Thrombocytopenia 2
SLC26A2
Atelosteogenesis, Type Ii
RHBDF2
Howel–evans Syndrome
SHH
Holoprosencephaly
SIX3
Holoprosencephaly
TGIF1
Holoprosencephaly
GLI2
Holoprosencephaly
IFIH1
Singleton Merten Syndrome
NODAL
Holoprosencephaly
NRAS
Neurocutaneous Melanosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
Holoprosencephaly
ZIC2
Holoprosencephaly
CDON
Holoprosencephaly