Disproportionate short-trunk short stature

Symptom Information:

Symptom ID: HPO:0003521
Synonyms:
Disproportionate short-trunked dwarfism [HPO:0003521]
Disproportionate short-trunked short stature [HPO:0003521]
Short trunk [HPO:0003521]
Short-trunked dwarfism [HPO:0003521]
Short trunk [OMIM:Short trunk]
Short-trunked dwarfism [OMIM:Short-trunked dwarfism]
Short stature, disproportionate short-trunked (identifiable at birth) [OMIM:Short stature, disproportionate short-trunked (identifiable at birth)]
Quality:
Cross references:
OMIM: "Short trunk" [OMIM:Short trunk]
OMIM: "Short-trunked dwarfism" [OMIM:Short-trunked dwarfism]
OMIM: "Short stature, disproportionate short-trunked (identifiable at birth)" [OMIM:Short stature, disproportionate short-trunked (identifiable at birth)]
Is a (Direct Parents):
HPO         Abnormal axial skeleton morphology
HPO         Disproportionate short stature
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Disproportionate short-trunk short stature(HPO:0003521)
       Growth abnormality(HPO:0001507)
          Growth delay(HPO:0001510)
             Short stature(HPO:0004322)
                Disproportionate short stature(HPO:0003498)
                   Disproportionate short-trunk short stature(HPO:0003521)
          Abnormality of body height(HPO:0000002)
             Short stature(HPO:0004322)
                Disproportionate short stature(HPO:0003498)
                   Disproportionate short-trunk short stature(HPO:0003521)
MedDRA:
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 2 (Orphanet:93296)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Brachyolmia type 1, Hobaek type (Orphanet:93301)
Brachyolmia type 1, Toledo type (Orphanet:93303)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Diaphanospondylodysostosis (Orphanet:66637)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Hypochondrogenesis (Orphanet:93297)
Kniest dysplasia (Orphanet:485)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
SMITH-MCCORT DYSPLASIA 2 (OMIM:615222)
SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE (OMIM:277300)
SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE (OMIM:608681)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE (OMIM:609223)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Smith-McCort dysplasia (Orphanet:178355)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloenchondrodysplasia (Orphanet:1855)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)