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Diseases
Genes (383)
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ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
MC2R
Familial Glucocorticoid Deficiency
TRNL1
Merrf Syndrome
LIPA
Acid Lipase Disease
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
STX3
Microvillus Inclusion Disease
IL1B
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
BRCA1
Primary Peritoneal Carcinoma
TRNK
Merrf Syndrome
ND5
Merrf Syndrome
TRNI
Merrf Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency