Irregular vertebral endplates
Symptom Information:
Symptom ID: | HPO:0003301 | |||||||||||||||||
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 axial skeleton morphology(HPO:0009121) Abnormality of the vertebral column(HPO:0000925) Abnormality of the vertebrae(HPO:0003468) Abnormal form of the vertebral bodies(HPO:0003312) Abnormality of the vertebral endplates(HPO:0005106) Irregular vertebral endplates(HPO:0003301) MedDRA: |
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Database Frequency: | 25 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Brachyolmia type 1, Toledo type | (Orphanet:93303) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
Czech dysplasia, metatarsal type | (Orphanet:137678) |
Dysosteosclerosis | (Orphanet:1782) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 | (OMIM:614135) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Hall-Riggs syndrome | (Orphanet:2107) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Metaphyseal chondrodysplasia, Schmid type | (Orphanet:174) |
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis | (Orphanet:93279) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Rhizomelic chondrodysplasia punctata type 2 | (Orphanet:309796) |
Roifman syndrome | (Orphanet:353298) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE | (OMIM:609223) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepimetaphyseal dysplasia, Pakistani type | (Orphanet:93282) |
Spondyloepiphyseal dysplasia tarda | (Orphanet:93284) |
THORACOLARYNGOPELVIC DYSPLASIA | (OMIM:187760) |
Thoracolaryngopelvic dysplasia | (Orphanet:3317) |
Wolcott-Rallison syndrome | (Orphanet:1667) |