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Diseases
Genes (332)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Hepatitis E
Viral Hemorrhagic Fevers
Singleton Merten Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
IFNG
Hepatitis E
Legionnaires' Disease
Yellow Fever
Viral Hemorrhagic Fevers
Vascular Tumor
RB1
Pinealoblastoma
Trilateral Retinoblastoma
COL9A2
Stickler Syndrome
DDX58
Hepatitis E
Viral Hemorrhagic Fevers
Singleton Merten Syndrome
TLR5
Legionnaires' Disease
COL9A1
Stickler Syndrome
GABRA5
Social (Pragmatic) Communication Disorder
SOST
Craniodiaphyseal Dysplasia
COL9A3
Stickler Syndrome
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
FLNA
Intestinal Neuronal Dysplasia