Mouth Diseases | Page 1

208 diseases found in 3 pages

2 Diseases

22q11.2 deletion syndrome

A Diseases

Ablepharon macrostomia syndrome Abruzzo-Erickson syndrome Acrodysostosis Acute necrotizing ulcerative gingivitis ADULT syndrome Ameloblastic carcinoma Amelogenesis imperfecta nephrocalcinosis Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Ankyloblepharon filiforme imperforate anus Ankylosis of teeth Anodontia Apert syndrome Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay Arthrogryposis multiplex congenita whistling face Atelosteogenesis type 1 Atelosteogenesis type 2 Atelosteogenesis type 3 Auriculo-condylar syndrome Ausems Wittebol-Post Hennekam syndrome

B Diseases

Bamforth syndrome Bifid nose Bixler Christian Gorlin syndrome Blepharo-cheilo-odontic syndrome Branchial arch syndrome X-linked Branchiooculofacial syndrome Branchiootorenal syndrome Bruck syndrome 1

C Diseases

Cardiomyopathy dilated with woolly hair and keratoderma Carey-Fineman-Ziter syndrome Catel Manzke syndrome CHARGE syndrome Charlie M syndrome Cherubism Childhood hypophosphatasia Chitayat Meunier Hodgkinson syndrome Classical-like Ehlers-Danlos syndrome Cleft hand absent tibia Cleft palate short stature vertebral anomalies Cleidocranial dysplasia Cleidocranial dysplasia recessive form Cone-rod dystrophy amelogenesis imperfecta Cornelia de Lange syndrome Crane-Heise syndrome

D Diseases

Deafness enamel hypoplasia nail defects Deafness oligodontia syndrome Dentatorubral-pallidoluysian atrophy Dentin dysplasia, coronal Dentin dysplasia sclerotic bones Dentin dysplasia, type 1 Dentinogenesis imperfecta Dentinogenesis imperfecta type 2 Dentinogenesis imperfecta type 3 Dermoodontodysplasia Diamond-Blackfan anemia

E Diseases

Ectodermal dysplasia trichoodontoonychial type Ectodermal dysplasia with natal teeth Turnpenny type EEC syndrome

F Diseases

Femoral facial syndrome Fetal hydantoin syndrome Fetal indomethacin syndrome Fetal methylmercury syndrome Fetal minoxidil syndrome Fetal valproate syndrome Florid cemento-osseous dysplasia Fragile X syndrome Frontofacionasal dysplasia Frontonasal dysplasia Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome Frontorhiny Fryns syndrome Fuhrmann syndrome

G Diseases

GAPO syndrome Generalized junctional epidermolysis bullosa, non-Herlitz type Genito palato cardiac syndrome Gingival fibromatosis, 1 Gingival fibromatosis, 2 Gingival fibromatosis, 3 Gingival fibromatosis, 4 Gingival fibromatosis with hypertrichosis Goldberg-Shprintzen megacolon syndrome Goldenhar disease Gordon syndrome

H Diseases

Haim-Munk syndrome Hanhart syndrome Hardikar syndrome Hemi 3 syndrome Hemifacial hyperplasia strabismus Hemifacial microsomia Hemifacial myohyperplasia Hyaline fibromatosis syndrome Hydrocephalus-cleft palate-joint contractures syndrome Hyperthermia induced defects Hypophosphatasia

I Diseases

Incontinentia pigmenti

J Diseases

Jones syndrome Juberg-Hayward syndrome Junctional epidermolysis bullosa generalized intermediate Junctional epidermolysis bullosa, Herlitz type

K Diseases

Kabuki syndrome

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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