Short long bone

Symptom Information:

Symptom ID: HPO:0003026
Synonyms:
Long bone shortening [HPO:0003026]
Short tubular bones [HPO:0003026]
shortened long tubular bones [HPO:0003026]
Long bone shortening [OMIM:Long bone shortening]
Short long bones [OMIM:Short long bones]
Short tubular bones [OMIM:Short tubular bones]
Shortened long tubular bones [OMIM:Shortened long tubular bones]
Short long bones (rhizomelic shortening) [OMIM:Short long bones (rhizomelic shortening)]
Short, long bones [OMIM:Short, long bones]
Short, tubular bones [OMIM:Short, tubular bones]
Shortened long bones [OMIM:Shortened long bones]
Quality:
Cross references:
OMIM: "Long bone shortening" [OMIM:Long bone shortening]
OMIM: "Short long bones" [OMIM:Short long bones]
OMIM: "Short tubular bones" [OMIM:Short tubular bones]
OMIM: "Shortened long tubular bones" [OMIM:Shortened long tubular bones]
OMIM: "Short long bones (rhizomelic shortening)" [OMIM:Short long bones (rhizomelic shortening)]
OMIM: "Short, long bones" [OMIM:Short, long bones]
OMIM: "Short, tubular bones" [OMIM:Short, tubular bones]
OMIM: "Shortened long bones" [OMIM:Shortened long bones]
Is a (Direct Parents):
HPO         Abnormality of long bone morphology
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:
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)