Premature loss of teeth
Symptom Information:
Symptom ID: | HPO:0006480 | ||||||||||||
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) Premature loss of teeth(HPO:0006480) MedDRA: |
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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) |