Enlarged epiphyses
Symptom Information:
Symptom ID: | HPO:0010580 | ||||||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormality of long bone morphology(HPO:0011314) Abnormality of epiphysis morphology(HPO:0005930) Enlarged epiphyses(HPO:0010580) MedDRA: |
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Database Frequency: | 14 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Dent disease type 1 | (Orphanet:93622) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Keipert syndrome | (Orphanet:2662) |
Progressive pseudorheumatoid arthropathy of childhood | (Orphanet:1159) |
SHORT syndrome | (Orphanet:3163) |
Spondylo-megaepiphyseal-metaphyseal dysplasia | (Orphanet:228387) |
Stickler syndrome type 3 | (Orphanet:166100) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B | (OMIM:600081) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
Weissenbacher- Zweymuller syndrome | (Orphanet:3450) |