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Diseases
Genes (824)
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BEST1
Vitelliform Macular Dystrophy
Degenerative Disease
Limb–girdle Muscular Dystrophy
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
LMNA
Degenerative Disease
Limb–girdle Muscular Dystrophy
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
GNE
Limb–girdle Muscular Dystrophy
Salla Disease
DMPK
Myotonic Dystrophy
AGGF1
Klippel-Trenaunay Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
Degenerative Disease
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy