Your browser does not support javascript:   Search for gard hereSearch for news-and-events here.

Diseases

Genetic and Rare Diseases Information Center (GARD)

Search for Rare or Genetic Diseases


Mouth Diseases

* This symbol indicates that a condition is not rare but is one for which a question has been answered by the GARD Information Center.

Is Rare Condition? Disease Name
* 22q11.2 deletion syndrome
* Aase-Smith syndrome
* Ablepharon macrostomia syndrome
* Abruzzo Erickson syndrome
* Ackerman syndrome
* Acrodysostosis
* Acute necrotizing ulcerative gingivitis
* ADULT syndrome
* Amelogenesis imperfecta nephrocalcinosis
* Ankyloblepharon filiforme imperforate anus
* Ankylosis of teeth
* Anodontia
* Apert syndrome
* Arthrogryposis multiplex congenita whistling face
* Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
* Atelosteogenesis type 1
* Atelosteogenesis type 2
* Atelosteogenesis type 3
* Auriculo-condylar syndrome
* Ausems Wittebol-Post Hennekam syndrome
* Bamforth syndrome
* Bixler Christian Gorlin syndrome
* Branchial arch syndrome X-linked
* Branchiooculofacial syndrome
* Branchiootorenal syndrome
* Bruck syndrome 1
* Catel Manzke syndrome
* CHARGE syndrome
* Charlie M syndrome
* Cherubism
* Chitayat Meunier Hodgkinson syndrome
* Cleft hand absent tibia
* Cleft palate short stature vertebral anomalies
* Cleidocranial dysplasia
* Cone-rod dystrophy amelogenesis imperfecta
* Congenital nonprogressive myopathy with Moebius and Robin sequences
* Cornelia de Lange syndrome
* Crane-Heise syndrome
* Deafness enamel hypoplasia nail defects
* Deafness oligodontia syndrome
* Dentatorubral-pallidoluysian atrophy
* Dentin dysplasia sclerotic bones
* Dentinogenesis imperfecta 1
* Dentinogenesis imperfecta Shields type 3
* Dermoodontodysplasia
* Diamond-Blackfan anemia
* Ectodermal dysplasia trichoodontoonychial type
* Ectodermal dysplasia with natal teeth Turnpenny type
* Femoral facial syndrome
* Fetal hydantoin syndrome
* Fetal valproate syndrome
* Florid cemento-osseous dysplasia
* Fragile X syndrome
* Frontofacionasal dysplasia
* Frontonasal dysplasia
* Fryns syndrome
* Fuhrmann syndrome
* GAPO syndrome
* Genito palato cardiac syndrome
* Gingival fibromatosis with hypertrichosis
* Gingival fibromatosis, 1
* Gingival fibromatosis, 2
* Gingival fibromatosis, 3
* Gingival fibromatosis, 4
* Goldberg-Shprintzen megacolon syndrome
* Gordon syndrome
* Haim-Munk syndrome
* Hanhart syndrome
* Hardikar syndrome
* Hay-Wells syndrome
* Hemi 3 syndrome
* Hemifacial hyperplasia strabismus
* Hemifacial microsomia
* Hemifacial myohyperplasia
* Hyperthermia induced defects
* Illum syndrome
* Jones syndrome
* Juberg-Hayward syndrome
* Junctional epidermolysis bullosa, Herlitz type
* Junctional epidermolysis bullosa, non-Herlitz type
* Juvenile hyaline fibromatosis
* Kabuki syndrome
* Kapur Toriello syndrome
* KBG syndrome
* Kniest dysplasia
* Kohlschutter Tonz syndrome
* Laband syndrome
* Lacrimo-auriculo-dento-digital syndrome
* Lambert syndrome
* Larsen syndrome
* Laryngoonychocutaneous syndrome
* Macroglossia
* Macrosomia with lethal microphthalmia
* Malignant hyperthermia arthrogryposis torticollis
* Marden Walker like syndrome
* Marden-Walker syndrome
* Maternal hyperphenylalaninemia
* Maxillonasal dysplasia, Binder type
* Meckel syndrome
* Medeira-Dennis-Donnai syndrome
* Median cleft of upper lip with polyps of facial skin and nasal mucosa
* Methimazole antenatal infection
* Methyl mercury antenatal infection
* Microbrachycephaly ptosis cleft lip
* Miller syndrome
* Moebius syndrome
* Multiple familial trichoepithelioma 1
* Nager acrofacial dysostosis
* Nance-Horan syndrome
* Native American myopathy
* Oculoauriculofrontonasal syndrome
* Oculocerebral syndrome with hypopigmentation
* Oculodentodigital dysplasia
* Oculofaciocardiodental syndrome
* Oculomaxillofacial dysostosis
* Odonto onycho dysplasia with alopecia
* Odontoma dysphagia syndrome
* Odontomicronychial dysplasia
* Odontoonychodermal dysplasia
* Omphalocele cleft palate syndrome lethal
* Oral submucous fibrosis
* Orofaciodigital syndrome 1
* Orofaciodigital syndrome 10
* Orofaciodigital syndrome 11
* Orofaciodigital syndrome 2
* Orofaciodigital syndrome 3
* Orofaciodigital syndrome 4
* Orofaciodigital syndrome 5
* Orofaciodigital syndrome 6
* Orofaciodigital syndrome 8
* Orofaciodigital syndrome 9
* Osteogenesis imperfecta type 3
* Osteogenesis imperfecta type 4
* Osteogenesis imperfecta type 6
* Oto-palato-digital syndrome type 1
* Oto-palato-digital syndrome type 2
* Otodental dysplasia
* Pallister W syndrome
* Papillon Lefevre syndrome
* Phenobarbital antenatal infection
* Pierre Robin sequence
* Pilodental dysplasia with refractive errors
* Pinheiro Freire-Maia Miranda syndrome
* Polydactyly cleft lip palate psychomotor retardation
* Popliteal pterygium syndrome lethal type
* Proteus syndrome
* Proximal chromosome 18q deletion syndrome
* Ramon Syndrome
* Rapadilino syndrome
* Richieri Costa Pereira syndrome
* Roberts syndrome
* Rutherfurd syndrome
* Say syndrome
* Simpson-Golabi-Behmel syndrome
* Single upper central incisor
* Smith-Lemli-Opitz syndrome type 1
* Smith-Magenis syndrome
* Spondylometaphyseal dysplasia with dentinogenesis imperfecta
* Steatocystoma multiplex with natal teeth
* Stickler syndrome type 1
* Stickler syndrome, type 2
* Stickler syndrome, type 3
* Sturge-Weber syndrome
* Syngnathia cleft palate
* Taurodontia absent teeth sparse hair
* Taurodontism
* Toriello Carey syndrome
* Treacher Collins syndrome
* Tricho-dento-osseous syndrome
* Trichodental syndrome
* Van der Woude syndrome
* Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence
* Verloes Bourguignon syndrome
* Verloove Vanhorick Brubakk syndrome
* Waardenburg syndrome type 1
* Waardenburg syndrome type 2
* Waardenburg syndrome type 3
* Weissenbacher-Zweymuller syndrome
* Witkop syndrome
* Xanthogranulomatous sialadenitis