Delayed epiphyseal ossification
Symptom Information:
Symptom ID: | HPO:0002663 | ||||||||||
Synonyms: |
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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) Abnormal bone structure(HPO:0003330) Abnormal bone ossification(HPO:0011849) Abnormal epiphyseal ossification(HPO:0010656) Delayed epiphyseal ossification(HPO:0002663) Abnormality of long bone morphology(HPO:0011314) Abnormality of epiphysis morphology(HPO:0005930) Delayed epiphyseal ossification(HPO:0002663) MedDRA: |
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Database Frequency: | 21 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Dent disease type 1 | (Orphanet:93622) |
Dyssegmental dysplasia - glaucoma | (Orphanet:1804) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 | (OMIM:600969) |
Eiken syndrome | (Orphanet:79106) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Kniest dysplasia | (Orphanet:485) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Pseudoachondroplasia | (Orphanet:750) |
SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION | (OMIM:182255) |
Short stature, Brussels type | (Orphanet:2867) |
Spondyloepimetaphyseal dysplasia - hypotrichosis | (Orphanet:168443) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
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) |