Natal tooth

Symptom Information:

Symptom ID: HPO:0000695
Synonyms:
Natal teeth [HPO:0000695]
Neonatal teeth [HPO:0000695]
Neonatal tooth (disorder) [Orphanet:12700]
Natal tooth (disorder) [Orphanet:12700]
Natal Teeth [Orphanet:12700]
Neonatal tooth [Orphanet:12700]
Natal teeth [OMIM:Natal teeth]
Neonatal teeth [OMIM:Neonatal teeth]
Premature eruption of teeth/natal teeth [Orphanet:12700]
Natal teeth [Orphanet:12700]
Tooth development disorder [MedDRA:10044030]
Disorders of tooth development and eruption [MedDRA:10044030]
Disturbances in tooth eruption [MedDRA:10044030]
Disturbances of tooth formation [MedDRA:10044030]
Other specified disorders of tooth development and eruption [MedDRA:10044030]
Unspecified disorder of tooth development and eruption [MedDRA:10044030]
Natal teeth [MedDRA:10044030]
Eruption of natal teeth [MedDRA:10044030]
Natal teeth (in some patients) [OMIM:Natal teeth (in some patients)]
Quality:
Cross references:
Orphanet:12700 "Premature eruption of teeth/natal teeth" [Orphanet:12700]
OMIM: "Natal teeth" [OMIM:Natal teeth]
OMIM: "Neonatal teeth" [OMIM:Neonatal teeth]
OMIM: "Natal teeth (in some patients)" [OMIM:Natal teeth (in some patients)]
UMLS:C0027443 "Natal Teeth" [Orphanet:12700]
UMLS:C0266049 "Neonatal tooth" [Orphanet:12700]
Is a (Direct Parents):
HPO         Advanced eruption of teeth
Orphanet Abnormality of the teeth
MedDRA Dental developmental disorders and anomalies
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)
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)