Abnormality of dental morphology
Symptom Information:
Symptom ID: | HPO:0006482 | |||||||||
Synonyms: |
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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) MedDRA: |
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Database Frequency: | 81 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
ADULT syndrome | (Orphanet:978) |
Abruzzo-Erickson syndrome | (Orphanet:921) |
Ackerman syndrome | (Orphanet:2561) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Atypical dentin dysplasia due to SMOC2 deficiency | (Orphanet:314721) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharoptosis - cleft palate - ectrodactyly - dental anomalies | (Orphanet:1258) |
CODAS syndrome | (Orphanet:1458) |
Cherubism | (Orphanet:184) |
Coffin-Lowry syndrome | (Orphanet:192) |
Deafness - onychodystrophy | (Orphanet:3231) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Dentin dysplasia | (Orphanet:1653) |
Distal monosomy 6p | (Orphanet:96125) |
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT | (OMIM:129490) |
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:224900) |
EEM syndrome | (Orphanet:1897) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fried's tooth and nail syndrome | (Orphanet:99672) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
Fukuda-Miyanomae-Nakata syndrome | (Orphanet:2060) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Hennekam syndrome | (Orphanet:2136) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypodontia - dysplasia of nails | (Orphanet:2228) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Incontinentia pigmenti | (Orphanet:464) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Ito hypomelanosis | (Orphanet:435) |
Kabuki syndrome | (Orphanet:2322) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
Microphthalmia, Lenz type | (Orphanet:568) |
Mikati-Najjar-Sahli syndrome | (Orphanet:2558) |
Non-eruption of teeth - maxillary hypoplasia - genu valgum | (Orphanet:2972) |
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:257850) |
Oculotrichodysplasia | (Orphanet:2718) |
Odonto-onycho dysplasia - alopecia | (Orphanet:2722) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Oligodontia | (Orphanet:99798) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
Otodental syndrome | (Orphanet:2791) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Pycnodysostosis | (Orphanet:763) |
Renal-genital-middle ear anomalies | (Orphanet:1092) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Syndromic X-linked intellectual deficit 7 | (Orphanet:85274) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
Treacher-Collins syndrome | (Orphanet:861) |
Tricho-dento-osseous syndrome | (Orphanet:3352) |
Trichodermodysplasia - dental alterations | (Orphanet:3353) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weaver-Williams syndrome | (Orphanet:3448) |
Weill-Marchesani syndrome | (Orphanet:3449) |
Williams syndrome | (Orphanet:904) |
Wrinkly skin syndrome | (Orphanet:2834) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |
Zunich-Kaye syndrome | (Orphanet:3474) |