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Diseases
Genes (845)
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DSPP
Dentin Dysplasia Type Ii
Dentin Dysplasia
Dentinogenesis Imperfecta
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Pectus Excavatum
Renpenning's Syndrome
MED12
Pectus Excavatum
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
PTH1R
Failure Of Eruption Of Teeth
FLNA
Pectus Excavatum
Intestinal Neuronal Dysplasia
Fg Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
BRAF
Pectus Excavatum
Erdheim–chester Disease
CTNS
Cystinosis
MMP20
Dentin Dysplasia
Dentinogenesis Imperfecta
RB1
Pinealoblastoma
Trilateral Retinoblastoma