Persistence of primary teeth
Symptom Information:
Symptom ID: | HPO:0006335 | ||||||||||||
Synonyms: |
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Quality: | |||||||||||||
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 primary teeth(HPO:0006481) Persistence of primary teeth(HPO:0006335) Abnormality of dental eruption(HPO:0006292) Persistence of primary teeth(HPO:0006335) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Dental disorders NEC(MedDRA:10044037) Persistence of primary teeth(HPO:0006335) |
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Database Frequency: | 12 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Carpenter syndrome | (Orphanet:65759) |
FAILURE OF TOOTH ERUPTION, PRIMARY | (OMIM:125350) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Kleefstra syndrome | (Orphanet:261494) |
MELAS | (Orphanet:550) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 | (OMIM:259710) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Pycnodysostosis | (Orphanet:763) |