Short long bone
Symptom Information:
Symptom ID: | HPO:0003026 | |||||||||||
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) Short long bone(HPO:0003026) MedDRA: |
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Database Frequency: | 51 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Achondrogenesis type 2 | (Orphanet:93296) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Acromicric dysplasia | (Orphanet:969) |
Brachydactyly type B | (Orphanet:93383) |
Brachyolmia type 1, Hobaek type | (Orphanet:93301) |
DESBUQUOIS DYSPLASIA 2 | (OMIM:615777) |
Diastrophic dwarfism | (Orphanet:628) |
Dyssegmental dysplasia - glaucoma | (Orphanet:1804) |
Dyssegmental dysplasia, Rolland-Desbuquois type | (Orphanet:156731) |
Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Fibrochondrogenesis | (Orphanet:2021) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
Geleophysic dysplasia | (Orphanet:2623) |
Goldblatt syndrome | (Orphanet:166272) |
Hypochondrogenesis | (Orphanet:93297) |
Hypochondroplasia | (Orphanet:429) |
Laron syndrome | (Orphanet:633) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
MUCOLIPIDOSIS III ALPHA/BETA | (OMIM:252600) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucolipidosis type 3 | (Orphanet:577) |
Myhre syndrome | (Orphanet:2588) |
Opsismodysplasia | (Orphanet:2746) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
Pseudoachondroplasia | (Orphanet:750) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE | (OMIM:611702) |
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE | (OMIM:613320) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Short-rib thoracic dysplasia 11 with or without polydactyly | (OMIM:615633) |
Short-rib thoracic dysplasia 3 with or without polydactyly | (OMIM:613091) |
Short-rib thoracic dysplasia 4 with or without polydactyly | (OMIM:613819) |
Short-rib thoracic dysplasia 7 with or without polydactyly | (OMIM:614091) |
Short-rib thoracic dysplasia 8 with or without polydactyly | (OMIM:615503) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia, matrilin-3 type | (Orphanet:156728) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Spondylometaphyseal dysplasia, Schmidt type | (Orphanet:93316) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |