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Diseases
Genes (668)
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TTPA
Familial Isolated Vitamin E Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
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
RET
Potter Sequence
IFIH1
Singleton Merten Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
PAH
Phenylketonuria
ITGA8
Potter Sequence
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
TNF
Diverticulum
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Latent Tuberculosis
Pleural Effusion
RB1
Pinealoblastoma
Trilateral Retinoblastoma
GREB1L
Potter Sequence
FREM1
Potter Sequence