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Diseases
Genes (628)
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AFG3L2
Spinocerebellar Ataxia Type 28
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TGM1
Bathing Suit Ichthyosis
ACTG2
Berdon Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ALOX12B
Bathing Suit Ichthyosis
ABCA12
Bathing Suit Ichthyosis