Disproportionate short-limb short stature

Symptom Information:

Symptom ID: HPO:0008873
Synonyms:
Brachymelic dwarfism [HPO:0008873]
Disproportionate short limb dwarfism [HPO:0008873]
Dwarfism, short-limbed [HPO:0008873]
Micromelic dwarfism [HPO:0008873]
SHORT LIMB DWARFISM [HPO:0008873]
Short limb dwarfism, disproportionate [HPO:0008873]
Short stature, disproportionate short limb [HPO:0008873]
Short stature, disproportionate short-limb [HPO:0008873]
Short-limb dwarfism [HPO:0008873]
Short-limbed dwarfism [HPO:0008873]
Dwarfism, short-limbed [OMIM:Dwarfism, short-limbed]
Short limb dwarfism [OMIM:Short limb dwarfism]
Short limb dwarfism, disproportionate [OMIM:Short limb dwarfism, disproportionate]
Short stature, disproportionate short limb [OMIM:Short stature, disproportionate short limb]
Short stature, disproportionate short-limb [OMIM:Short stature, disproportionate short-limb]
Short-limb dwarfism [OMIM:Short-limb dwarfism]
Short-limbed dwarfism [OMIM:Short-limbed dwarfism]
Brachymelic dwarfism (upper limbs greater than lower limbs) [OMIM:Brachymelic dwarfism (upper limbs greater than lower limbs)]
Dwarfism, disproportionate short-limb [OMIM:Dwarfism, disproportionate short-limb]
Dwarfism, micromelic [OMIM:Dwarfism, micromelic]
Dwarfism, short-limb [OMIM:Dwarfism, short-limb]
Short stature, disproportionate short-limbed (dwarfism) [OMIM:Short stature, disproportionate short-limbed (dwarfism)]
Quality:
Cross references:
OMIM: "Dwarfism, short-limbed" [OMIM:Dwarfism, short-limbed]
OMIM: "Short limb dwarfism" [OMIM:Short limb dwarfism]
OMIM: "Short limb dwarfism, disproportionate" [OMIM:Short limb dwarfism, disproportionate]
OMIM: "Short stature, disproportionate short limb" [OMIM:Short stature, disproportionate short limb]
OMIM: "Short stature, disproportionate short-limb" [OMIM:Short stature, disproportionate short-limb]
OMIM: "Short-limb dwarfism" [OMIM:Short-limb dwarfism]
OMIM: "Short-limbed dwarfism" [OMIM:Short-limbed dwarfism]
OMIM: "Brachymelic dwarfism (upper limbs greater than lower limbs)" [OMIM:Brachymelic dwarfism (upper limbs greater than lower limbs)]
OMIM: "Dwarfism, disproportionate short-limb" [OMIM:Dwarfism, disproportionate short-limb]
OMIM: "Dwarfism, micromelic" [OMIM:Dwarfism, micromelic]
OMIM: "Dwarfism, short-limb" [OMIM:Dwarfism, short-limb]
OMIM: "Short stature, disproportionate short-limbed (dwarfism)" [OMIM:Short stature, disproportionate short-limbed (dwarfism)]
Is a (Direct Parents):
HPO         Disproportionate 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)
                   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:
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)