Microdontia
Symptom Information:
Symptom ID: | HPO:0000691 | |||||||||||
Synonyms: |
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Quality: | ||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |