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Diseases
Genes (436)
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ASL
Argininosuccinic Aciduria
Hyperoxia
TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ASS1
Argininosuccinic Aciduria
Hyperoxia
Citrullinemia Type I
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CYP1A1
Hyperoxia
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CNBP
Myotonic Dystrophy
BRAF
Erdheim–chester Disease
LEMD3
Pmm2 Deficiency
Melorheostosis