Natal tooth
Symptom Information:
Symptom ID: | HPO:0000695 | |||||||||||||||||||
Synonyms: |
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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 eruption(HPO:0006292) Advanced eruption of teeth(HPO:0006288) Natal tooth(HPO:0000695) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Dental developmental disorders and anomalies(MedDRA:10012321) Natal tooth(HPO:0000695) |
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Database Frequency: | 42 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
CRANIOMETADIAPHYSEAL DYSPLASIA | (OMIM:269300) |
Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
Coffin-Lowry syndrome | (Orphanet:192) |
Craniometadiaphyseal dysplasia, wormian bone type | (Orphanet:85184) |
Dysosteosclerosis | (Orphanet:1782) |
Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Eosinophilic granuloma | (Orphanet:99871) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Fused mandibular incisors | (Orphanet:2287) |
Gnathodiaphyseal dysplasia | (Orphanet:53697) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hypertelorism, Teebi type | (Orphanet:1519) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Kleefstra syndrome | (Orphanet:261494) |
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Natal teeth - intestinal pseudoobstruction - patent ductus | (Orphanet:1654) |
Odonto-tricho-ungual-digito-palmar syndrome | (Orphanet:69082) |
Odontomicronychial dysplasia | (Orphanet:1811) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PACHYONYCHIA CONGENITA 2 | (OMIM:167210) |
Pallister-Hall syndrome | (Orphanet:672) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
SENER SYNDROME | (OMIM:606156) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Short-rib thoracic dysplasia 13 with or without polydactyly | (OMIM:616300) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Sotos syndrome | (Orphanet:821) |
Steatocystoma multiplex - natal teeth | (Orphanet:3184) |
Stickler syndrome | (Orphanet:828) |
TEETH PRESENT AT BIRTH | (OMIM:187050) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |