Premature loss of teeth

Symptom Information:

Symptom ID: HPO:0006480
Synonyms:
Early tooth loss [HPO:0006480]
Loss of teeth [HPO:0006480]
Premature teeth loss [HPO:0006480]
Premature tooth loss [HPO:0006480]
Early tooth loss [OMIM:Early tooth loss]
Loss of teeth [OMIM:Loss of teeth]
Premature loss of teeth [OMIM:Premature loss of teeth]
Premature teeth loss [OMIM:Premature teeth loss]
Premature tooth loss [OMIM:Premature tooth loss]
Early teeth loss [OMIM:Early teeth loss]
Early tooth loss (third decade) [OMIM:Early tooth loss (third decade)]
Premature tooth loss (both primary and secondary dentition) [OMIM:Premature tooth loss (both primary and secondary dentition)]
Quality:
Cross references:
OMIM: "Early tooth loss" [OMIM:Early tooth loss]
OMIM: "Loss of teeth" [OMIM:Loss of teeth]
OMIM: "Premature loss of teeth" [OMIM:Premature loss of teeth]
OMIM: "Premature teeth loss" [OMIM:Premature teeth loss]
OMIM: "Premature tooth loss" [OMIM:Premature tooth loss]
OMIM: "Early teeth loss" [OMIM:Early teeth loss]
OMIM: "Early tooth loss (third decade)" [OMIM:Early tooth loss (third decade)]
OMIM: "Premature tooth loss (both primary and secondary dentition)" [OMIM:Premature tooth loss (both primary and secondary dentition)]
Is a (Direct Parents):
HPO         Abnormality of the teeth
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)
                         Premature loss of teeth(HPO:0006480)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

ANE syndrome (Orphanet:157954)
Chronic mucocutaneous candidiasis (Orphanet:1334)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dyskeratosis congenita (Orphanet:1775)
Dysosteosclerosis (Orphanet:1782)
Ehlers-Danlos syndrome, periodontitis type (Orphanet:75392)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial expansile osteolysis (Orphanet:85195)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Juvenile Paget disease (Orphanet:2801)
MELAS (Orphanet:550)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
NEUTROPENIA, CHRONIC FAMILIAL (OMIM:162700)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculodentodigital dysplasia (Orphanet:2710)
PERIODONTITIS, AGGRESSIVE, 1 (OMIM:170650)
Papillon-Lefèvre syndrome (Orphanet:678)