Disproportionate short stature

Symptom Information:

Symptom ID: HPO:0003498
Synonyms:
Short stature, disproportionate [HPO:0003498]
SHORT STATURE, SEVERE DISPROPORTIONATE [HPO:0003498]
Short stature, disproportionate [OMIM:Short stature, disproportionate]
Short stature, severe disproportionate [OMIM:Short stature, severe disproportionate]
Short stature, disproportionate (short lower limbs) [OMIM:Short stature, disproportionate (short lower limbs)]
Short stature, disproportionate (short trunk) [OMIM:Short stature, disproportionate (short trunk)]
Quality:
Cross references:
OMIM: "Short stature, disproportionate" [OMIM:Short stature, disproportionate]
OMIM: "Short stature, severe disproportionate" [OMIM:Short stature, severe disproportionate]
OMIM: "Short stature, disproportionate (short lower limbs)" [OMIM:Short stature, disproportionate (short lower limbs)]
OMIM: "Short stature, disproportionate (short trunk)" [OMIM:Short stature, disproportionate (short trunk)]
Is a (Direct Parents):
HPO         Short stature
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)
          Growth delay(HPO:0001510)
             Short stature(HPO:0004322)
                Disproportionate short stature(HPO:0003498)
MedDRA:
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)