Microdontia

Symptom Information:

Symptom ID: HPO:0000691
Synonyms:
Small teeth [HPO:0000691]
Microdontia (disorder) [Orphanet:12150]
Microdontia [Orphanet:12150]
Microdontia [OMIM:Microdontia]
Small teeth [OMIM:Small teeth]
Complete/partial microdontia [Orphanet:12150]
Microdontia (in some patients) [OMIM:Microdontia (in some patients)]
Microdontia (maxillary lateral incisors) [OMIM:Microdontia (maxillary lateral incisors)]
Small teeth (classic feature) [OMIM:Small teeth (classic feature)]
Small teeth (in some patients) [OMIM:Small teeth (in some patients)]
Teeth small [OMIM:Teeth small]
Quality:
Cross references:
HPO:0006307 "Small, widely spaced teeth" [Orphanet:12150]
Orphanet:12150 "Complete/partial microdontia" [Orphanet:12150]
OMIM: "Microdontia" [OMIM:Microdontia]
OMIM: "Small teeth" [OMIM:Small teeth]
OMIM: "Microdontia (in some patients)" [OMIM:Microdontia (in some patients)]
OMIM: "Microdontia (maxillary lateral incisors)" [OMIM:Microdontia (maxillary lateral incisors)]
OMIM: "Small teeth (classic feature)" [OMIM:Small teeth (classic feature)]
OMIM: "Small teeth (in some patients)" [OMIM:Small teeth (in some patients)]
OMIM: "Teeth small" [OMIM:Teeth small]
UMLS:C0240340 "Microdontia" [HPO:0000691]
UMLS:C0240340 "Microdontia" [Orphanet:12150]
Is a (Direct Parents):
Orphanet Abnormality of the teeth
HPO         Abnormality of dental morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the teeth(HPO:0000164)
                         Abnormality of dental morphology(HPO:0006482)
                            Microdontia(HPO:0000691)
MedDRA:
Database Frequency: 104 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
AMELOGENESIS IMPERFECTA, TYPE IE (OMIM:301200)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
AXENFELD-RIEGER SYNDROME, TYPE 3 (OMIM:602482)
Ablepharon macrostomia syndrome (Orphanet:920)
Atkin-Flaitz syndrome (Orphanet:1193)
Atypical dentin dysplasia due to SMOC2 deficiency (Orphanet:314721)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Axenfeld-Rieger syndrome (Orphanet:782)
BOR syndrome (Orphanet:107)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Bowed tibiae - radial anomalies - osteopenia - fractures (Orphanet:3331)
Brachyolmia-amelogenesis imperfecta syndrome (Orphanet:2899)
Branchio-oculo-facial syndrome (Orphanet:1297)
CHST3-related skeletal dysplasia (Orphanet:263463)
CLARK-BARAITSER SYNDROME (OMIM:300602)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Cataract - hypertrichosis - intellectual deficit (Orphanet:1375)
Cerebellar ataxia - ectodermal dysplasia (Orphanet:1174)
Cole-Carpenter syndrome (Orphanet:2050)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Dermo-odonto dysplasia (Orphanet:1660)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Down syndrome (Orphanet:870)
Dyschondrosteosis - nephritis (Orphanet:1765)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Ellis Van Creveld syndrome (Orphanet:289)
Fetal alcohol syndrome (Orphanet:1915)
Filippi syndrome (Orphanet:3255)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
Johanson-Blizzard syndrome (Orphanet:2315)
Kabuki syndrome (Orphanet:2322)
Koolen-De Vries syndrome (Orphanet:96169)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Laron syndrome (Orphanet:633)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MEIER-GORLIN SYNDROME 5 (OMIM:613805)
Maxillo-nasal dysplasia (Orphanet:1248)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Moebius syndrome (Orphanet:570)
Mucolipidosis type 4 (Orphanet:578)
Mucopolysaccharidosis type 1 (Orphanet:579)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS (OMIM:257790)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Oculodentodigital dysplasia (Orphanet:2710)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odontotrichomelic syndrome (Orphanet:2723)
Oligodontia (Orphanet:99798)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Qazi-Markouizos syndrome (Orphanet:3010)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Rosselli-Gulienetti syndrome (Orphanet:90339)
Rothmund-Thomson syndrome (Orphanet:2909)
SECKEL SYNDROME 2 (OMIM:606744)
SHORT syndrome (Orphanet:3163)
SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH (OMIM:606895)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Shwachman-Diamond syndrome (Orphanet:811)
Stimmler syndrome (Orphanet:3199)
Subaortic stenosis - short stature (Orphanet:3191)
TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS (OMIM:313490)
TOOTH AGENESIS, SELECTIVE, 3 (OMIM:604625)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Temtamy preaxial brachydactyly syndrome (Orphanet:363417)
Tricho-dento-osseous syndrome (Orphanet:3352)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trisomy 20p (Orphanet:261318)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Usher syndrome (Orphanet:886)
Usher syndrome type 2 (Orphanet:231178)
Williams syndrome (Orphanet:904)
Wrinkly skin syndrome (Orphanet:2834)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)