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Diseases
Genes (558)
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TTPA
Familial Isolated Vitamin E Deficiency
Speech Disorder
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
MED12
Speech Disorder
Fg Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
CNBP
Myotonic Dystrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
FH
Fumarase Deficiency
Speech Disorder
GNAS
Heterotopic Ossification
NKX2-5
Myotonic Dystrophy