Mesomelic/rhizomelic limb shortening

Symptom Information:

Symptom ID: HPO:0005026
Synonyms:
Mesomelic/rhizomelic limb shortening [OMIM:Mesomelic/rhizomelic limb shortening]
Quality:
Cross references:
OMIM: "Mesomelic/rhizomelic limb shortening" [OMIM:Mesomelic/rhizomelic limb shortening]
Is a (Direct Parents):
HPO         Rhizomelia
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)
                      Rhizomelia(HPO:0008905)
                         Mesomelic/rhizomelic limb shortening(HPO:0005026)
          Growth delay(HPO:0001510)
             Short stature(HPO:0004322)
                Disproportionate short stature(HPO:0003498)
                   Disproportionate short-limb short stature(HPO:0008873)
                      Rhizomelia(HPO:0008905)
                         Mesomelic/rhizomelic limb shortening(HPO:0005026)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Limb undergrowth(HPO:0009826)
                         Rhizomelia(HPO:0008905)
                            Mesomelic/rhizomelic limb shortening(HPO:0005026)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Limb undergrowth(HPO:0009826)
                      Rhizomelia(HPO:0008905)
                         Mesomelic/rhizomelic limb shortening(HPO:0005026)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Bohring-Opitz syndrome (Orphanet:97297)
Tetrasomy 12p (Orphanet:884)