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Diseases
Genes (605)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Viral Hemorrhagic Fevers
Singleton Merten Syndrome
Severe Acute Respiratory Syndrome
LMNA
Limb–girdle Muscular Dystrophy
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy
DES
Limb–girdle Muscular Dystrophy
CAV3
Limb–girdle Muscular Dystrophy
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
DAG1
Viral Hemorrhagic Fevers
Limb–girdle Muscular Dystrophy
CTNS
Limb–girdle Muscular Dystrophy
Cystinosis
FKRP
Limb–girdle Muscular Dystrophy
POMT2
Limb–girdle Muscular Dystrophy
TTN
Limb–girdle Muscular Dystrophy