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Diseases
Genes (2045)
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ARSB
Mucopolysaccharidosis Type 6
ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
TRNL1
Merrf Syndrome
LIPA
Acid Lipase Disease
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
IL1B
Alopecia, Androgenetic, 1
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
Childhood Leukemia
TP53
Alopecia, Androgenetic, 1
Primary Peritoneal Carcinoma
Carcinoid Syndrome
Childhood Leukemia
ASS1
Citrullinemia Type I
BRCA1
Primary Peritoneal Carcinoma
Childhood Leukemia
PRKAR1A
Alopecia, Androgenetic, 1
Enamel-Renal Syndrome
Childhood Leukemia
AR
Alopecia, Androgenetic, 1
Tetraplegia
Childhood Leukemia
TRNK
Merrf Syndrome
SRD5A2
Alopecia, Androgenetic, 1
MTHFR
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
Tetraplegia
Childhood Leukemia