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Diseases
Genes (422)
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ASL
Argininosuccinic Aciduria
Hyperoxia
TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
MYH9
Arterial Tortuosity Syndrome
Myh9-Related Disease
PMM2
Pmm2 Deficiency
TNNI2
Sheldon-Hall Syndrome
SLC2A10
Hiatal Hernia
Arterial Tortuosity Syndrome
PQBP1
Renpenning's Syndrome
MYH3
Sheldon-Hall Syndrome
IFIH1
Singleton Merten Syndrome
TPM2
Sheldon-Hall Syndrome
TNNT3
Sheldon-Hall Syndrome
CYP1A1
Hyperoxia
RB1
Pinealoblastoma
Trilateral Retinoblastoma
COMT
Tmj Disorders
DDX58
Singleton Merten Syndrome
SPG29
Spastic Paraplegia 29, Autosomal Dominant
PDGFRA
Intussusception
Hyperoxia
COL1A1
Hiatal Hernia
Hernia
THAS
Hernia
C9
Favre–racouchot Syndrome