Childhood-onset short-trunk short stature

Symptom Information:

Symptom ID: HPO:0008922
Synonyms:
Disproportionate short stature (short trunk), identifiable in childhood [HPO:0008922]
Short-trunk dwarfism identifiable during childhood [HPO:0008922]
Short-trunk dwarfism identifiable during childhood [OMIM:Short-trunk dwarfism identifiable during childhood]
Quality:
Cross references:
OMIM: "Short-trunk dwarfism identifiable during childhood" [OMIM:Short-trunk dwarfism identifiable during childhood]
Is a (Direct Parents):
HPO         Disproportionate short-trunk 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)
                   Childhood-onset short-trunk short stature(HPO:0008922)
       Growth abnormality(HPO:0001507)
          Growth delay(HPO:0001510)
             Short stature(HPO:0004322)
                Disproportionate short stature(HPO:0003498)
                   Disproportionate short-trunk short stature(HPO:0003521)
                      Childhood-onset short-trunk short stature(HPO:0008922)
          Abnormality of body height(HPO:0000002)
             Short stature(HPO:0004322)
                Disproportionate short stature(HPO:0003498)
                   Disproportionate short-trunk short stature(HPO:0003521)
                      Childhood-onset short-trunk short stature(HPO:0008922)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Brachyolmia (Orphanet:1293)
Brachyolmia type 1, Toledo type (Orphanet:93303)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT (OMIM:184100)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)