Disproportionate short stature
Symptom Information:
Symptom ID: | HPO:0003498 | ||||||
Synonyms: |
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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) Growth delay(HPO:0001510) Short stature(HPO:0004322) Disproportionate short stature(HPO:0003498) Abnormality of body height(HPO:0000002) Short stature(HPO:0004322) Disproportionate short stature(HPO:0003498) MedDRA: |
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Database Frequency: | 28 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED | (OMIM:304950) |
Dysosteosclerosis | (Orphanet:1782) |
Kniest dysplasia | (Orphanet:485) |
Kyphomelic dysplasia | (Orphanet:1801) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
Madelung deformity | (Orphanet:35688) |
Metaphyseal chondrodysplasia, Spahr type | (Orphanet:2501) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
Pelviscapular dysplasia | (Orphanet:93333) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
Rhizomelic chondrodysplasia punctata type 2 | (Orphanet:309796) |
SMITH-MCCORT DYSPLASIA 1 | (OMIM:607326) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE | (OMIM:611702) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Short stature - valvular heart disease - characteristic facies | (Orphanet:2868) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |