Disproportionate short-limb short stature
Symptom Information:
Symptom ID: | HPO:0008873 | ||||||||||||||||||||||
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) Growth abnormality(HPO:0001507) Abnormality of body height(HPO:0000002) Short stature(HPO:0004322) Disproportionate short stature(HPO:0003498) Disproportionate short-limb short stature(HPO:0008873) Growth delay(HPO:0001510) Short stature(HPO:0004322) Disproportionate short stature(HPO:0003498) Disproportionate short-limb short stature(HPO:0008873) MedDRA: |
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Database Frequency: | 39 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
Achondrogenesis type 2 | (Orphanet:93296) |
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Acromesomelic dysplasia, Grebe type | (Orphanet:2098) |
Atelosteogenesis type I | (Orphanet:1190) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES | (OMIM:609441) |
Campomelic dysplasia | (Orphanet:140) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES | (OMIM:127200) |
Desbuquois syndrome | (Orphanet:1425) |
Diastrophic dwarfism | (Orphanet:628) |
Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
Greenberg dysplasia | (Orphanet:1426) |
Infantile hypophosphatasia | (Orphanet:247651) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Micromelic dwarfism, Fryns type | (Orphanet:2641) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
OSTEOGENESIS IMPERFECTA, TYPE II | (OMIM:166210) |
OSTEOGENESIS IMPERFECTA, TYPE IX | (OMIM:259440) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
Opsismodysplasia | (Orphanet:2746) |
Osteogenesis imperfecta type 2 | (Orphanet:216804) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Peters-plus syndrome | (Orphanet:709) |
Pseudoachondroplasia | (Orphanet:750) |
Rhizomelic chondrodysplasia punctata type 3 | (Orphanet:309803) |
SPONASTRIME dysplasia | (Orphanet:93357) |
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE | (OMIM:611702) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondyloepimetaphyseal dysplasia, matrilin-3 type | (Orphanet:156728) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Spondylometaphyseal dysplasia, A4 type | (Orphanet:168555) |
Thoracomelic dysplasia | (Orphanet:1803) |