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Diseases
Genes (644)
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GJA1
Oculodentodigital Dysplasia
F9
Haemophilia B
PMM2
Pmm2 Deficiency
EDA
Hypohidrotic Ectodermal Dysplasia
Periapical Cyst
MED12
Fg Syndrome
PQBP1
Renpenning's Syndrome
ABCC9
Cantú Syndrome
UMOD
Medullary Cystic Kidney Disease
FGF10
Aplasia Of Lacrimal And Salivary Glands
EDARADD
Hypohidrotic Ectodermal Dysplasia
KCNJ8
Cantú Syndrome
DMPK
Myotonic Dystrophy
ALPL
Odontohypophosphatasia
CNBP
Myotonic Dystrophy
EDAR
Hypohidrotic Ectodermal Dysplasia
BRAF
Oral Manifestations Of Systemic Disease
Erdheim–chester Disease
TCIRG1
Osteopetrosis, Autosomal Recessive 2
CLCN7
Dental Fluorosis
Osteopetrosis, Autosomal Recessive 2
MBTPS2
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant
CASK
Fg Syndrome