Premature loss of primary teeth
Symptom Information:
Symptom ID: | HPO:0006323 | |||||||
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) Premature loss of primary teeth(HPO:0006323) Abnormality of primary teeth(HPO:0006481) Premature loss of primary teeth(HPO:0006323) MedDRA: |
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Database Frequency: | 18 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Adult hypophosphatasia | (Orphanet:247676) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Childhood-onset hypophosphatasia | (Orphanet:247667) |
Ehlers-Danlos syndrome, periodontitis type | (Orphanet:75392) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Infantile hypophosphatasia | (Orphanet:247651) |
Kindler syndrome | (Orphanet:2908) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Odontohypophosphatasia | (Orphanet:247685) |
Odontomicronychial dysplasia | (Orphanet:1811) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Yunis-Varon syndrome | (Orphanet:3472) |