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Diseases
Genes (526)
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TTPA
Familial Isolated Vitamin E Deficiency
Dysmetria
FBN1
Weill-Marchesani Syndrome 3
ADAMTS10
Weill-Marchesani Syndrome 3
SLC12A6
Andermann Syndrome
NGLY1
Dysmetria
Ngly1 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
LTBP2
Weill-Marchesani Syndrome 3
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma