Irregular epiphyses
Symptom Information:
Symptom ID: | HPO:0010582 | |||
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) Irregular epiphyses(HPO:0010582) MedDRA: |
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Database Frequency: | 19 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Diastrophic dwarfism | (Orphanet:628) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 | (OMIM:600969) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 | (OMIM:614135) |
Goldblatt syndrome | (Orphanet:166272) |
Jeune syndrome | (Orphanet:474) |
Lowry-Wood syndrome | (Orphanet:1824) |
Microspherophakia - metaphyseal dysplasia | (Orphanet:2551) |
Multiple epiphyseal dysplasia due to collagen 9 anomaly | (Orphanet:166002) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Multiple epiphyseal dysplasia, Lowry type | (Orphanet:166016) |
Pseudoachondroplasia | (Orphanet:750) |
SMITH-MCCORT DYSPLASIA 1 | (OMIM:607326) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED | (OMIM:313400) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Smith-McCort dysplasia | (Orphanet:178355) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepimetaphyseal dysplasia, matrilin-3 type | (Orphanet:156728) |