Reduced number of teeth
Symptom Information:
Symptom ID: | HPO:0009804 | ||
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) Abnormal number of teeth(HPO:0006483) Reduced number of teeth(HPO:0009804) MedDRA: |
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Database Frequency: | 137 / 7739 | ||
Resource: |
All diseases associated with this symptom:
12q14 microdeletion syndrome | (Orphanet:94063) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Ankyloblepharon filiforme - imperforate anus | (Orphanet:1074) |
Anodontia | (Orphanet:99797) |
Arrhinia - choanal atresia - microphthalmia | (Orphanet:1135) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal dominant microcephaly | (Orphanet:2514) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Bloom syndrome | (Orphanet:125) |
Brachydactyly - mesomelia - intellectual deficit - heart defects | (Orphanet:1277) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Böök syndrome | (Orphanet:1262) |
CHARGE syndrome | (Orphanet:138) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Char syndrome | (Orphanet:46627) |
Charlie M syndrome | (Orphanet:1406) |
Cherubism | (Orphanet:184) |
Cleft lip/palate - deafness - sacral lipoma | (Orphanet:2003) |
Cleft palate - stapes fixation - oligodontia | (Orphanet:2010) |
Coffin-Lowry syndrome | (Orphanet:192) |
Cohen syndrome | (Orphanet:193) |
Congenital unilateral hypoplasia of depressor anguli oris | (Orphanet:1166) |
Cornelia de Lange syndrome | (Orphanet:199) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Craniofaciofrontodigital syndrome | (Orphanet:363705) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Craniosynostosis - fibular aplasia | (Orphanet:1533) |
Cutis gyrata - acanthosis nigricans - craniosynostosis | (Orphanet:1555) |
Deafness - oligodontia | (Orphanet:3230) |
Deafness - onychodystrophy | (Orphanet:3231) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Dental ankylosis | (Orphanet:1077) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Dermo-odonto dysplasia | (Orphanet:1660) |
Distal monosomy 6p | (Orphanet:96125) |
Dysostosis, Stanescu type | (Orphanet:1798) |
EEC syndrome | (Orphanet:1896) |
EEM syndrome | (Orphanet:1897) |
Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Epidermolysis bullosa simplex with anodontia/hypodontia | (Orphanet:2325) |
Extrasystoles - short stature - hyperpigmentation - microcephaly | (Orphanet:1964) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Focal dermal hypoplasia | (Orphanet:2092) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Hennekam syndrome | (Orphanet:2136) |
Holoprosencephaly | (Orphanet:2162) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hypodontia - dysplasia of nails | (Orphanet:2228) |
Hypoglossia - hypodactyly | (Orphanet:989) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Incontinentia pigmenti | (Orphanet:464) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
KBG syndrome | (Orphanet:2332) |
Kabuki syndrome | (Orphanet:2322) |
Kallmann syndrome | (Orphanet:478) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Laron syndrome | (Orphanet:633) |
Lowry-MacLean syndrome | (Orphanet:2409) |
MEHMO syndrome | (Orphanet:85282) |
Macrocephaly - short stature - paraplegia | (Orphanet:2427) |
Maxillo-nasal dysplasia | (Orphanet:1248) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Moebius syndrome | (Orphanet:570) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Non-eruption of teeth - maxillary hypoplasia - genu valgum | (Orphanet:2972) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculodental syndrome, Rutherfurd type | (Orphanet:2709) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Odonto-onycho dysplasia - alopecia | (Orphanet:2722) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Oligodontia | (Orphanet:99798) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Otodental syndrome | (Orphanet:2791) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Proteus syndrome | (Orphanet:744) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Seckel syndrome | (Orphanet:808) |
Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Smith-Magenis syndrome | (Orphanet:819) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
Stickler syndrome | (Orphanet:828) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Symptomatic form of Coffin-Lowry syndrome in female carriers | (Orphanet:276630) |
Taurodontia - absent teeth - sparse hair | (Orphanet:2731) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Treacher-Collins syndrome | (Orphanet:861) |
Tricho-odonto-onychial dysplasia | (Orphanet:3355) |
Tricho-retino-dento-digital syndrome | (Orphanet:1264) |
Trichodental syndrome | (Orphanet:3351) |
Trichodermodysplasia - dental alterations | (Orphanet:3353) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Van der Woude syndrome | (Orphanet:888) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
W syndrome | (Orphanet:2804) |
Weaver-Williams syndrome | (Orphanet:3448) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |
Zunich-Kaye syndrome | (Orphanet:3474) |