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Diseases
Genes (982)
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DSPP
Dentin Dysplasia Type Ii
Dentin Dysplasia
Dentinogenesis Imperfecta
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E 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
IFIH1
Myasthenia Gravis
Singleton Merten Syndrome
FLNA
Pectus Excavatum
Intestinal Neuronal Dysplasia
Fg Syndrome
ACTG2
Berdon Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
TNF
Adult-Onset Still's Disease
Myasthenia Gravis
Allergic Contact Dermatitis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Premenstrual Syndrome (Pms)
MYH11
Berdon Syndrome
IFNG
Adult-Onset Still's Disease
Myasthenia Gravis
Allergic Contact Dermatitis
Vascular Tumor
Dentinogenesis Imperfecta
Cystinosis
MYLK
Berdon Syndrome
CTNS
Cystinosis
IL10
Adult-Onset Still's Disease
Myasthenia Gravis
Allergic Contact Dermatitis
Premenstrual Syndrome (Pms)
Cystinosis
IL18
Adult-Onset Still's Disease
Allergic Contact Dermatitis
Cystinosis