Proportionate short stature
Symptom Information:
Symptom ID: | HPO:0003508 | ||||||
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) Proportionate short stature(HPO:0003508) Abnormality of body height(HPO:0000002) Short stature(HPO:0004322) Proportionate short stature(HPO:0003508) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
GMS syndrome | (Orphanet:2090) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS | (OMIM:609654) |
Seckel syndrome | (Orphanet:808) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondyloepiphyseal dysplasia, Kimberley type | (Orphanet:93283) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |