Small epiphyses
Symptom Information:
Symptom ID: | HPO:0010585 | ||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormality of long bone morphology(HPO:0011314) Abnormality of epiphysis morphology(HPO:0005930) Small epiphyses(HPO:0010585) MedDRA: |
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Database Frequency: | 16 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Anauxetic dysplasia | (Orphanet:93347) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 | (OMIM:600969) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 | (OMIM:614135) |
Goldblatt syndrome | (Orphanet:166272) |
Lowry-Wood syndrome | (Orphanet:1824) |
Metaphyseal anadysplasia | (Orphanet:1040) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Bieganski type | (Orphanet:168448) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepimetaphyseal dysplasia, matrilin-3 type | (Orphanet:156728) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Wolcott-Rallison syndrome | (Orphanet:1667) |