Proportionate short stature

Symptom Information:

Symptom ID: HPO:0003508
Synonyms:
Proportionate small stature [HPO:0003508]
Short stature, proportionate [HPO:0003508]
Proportionate short stature [OMIM:Proportionate short stature]
Proportionate small stature [OMIM:Proportionate small stature]
Short stature, proportionate [OMIM:Short stature, proportionate]
Short stature, proportionate (<5th percentile) [OMIM:Short stature, proportionate (<5th percentile)]
Quality:
Cross references:
OMIM: "Proportionate short stature" [OMIM:Proportionate short stature]
OMIM: "Proportionate small stature" [OMIM:Proportionate small stature]
OMIM: "Short stature, proportionate" [OMIM:Short stature, proportionate]
OMIM: "Short stature, proportionate (<5th percentile)" [OMIM:Short stature, proportionate (<5th percentile)]
Is a (Direct Parents):
HPO         Short stature
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:
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)