Upper limb undergrowth

Symptom Information:

Symptom ID: HPO:0009824
Synonyms:
Short arms [HPO:0009824]
Shortening of the arms [HPO:0009824]
Short arms [OMIM:Short arms]
Shortening of the arms [OMIM:Shortening of the arms]
Quality:
Cross references:
OMIM: "Short arms" [OMIM:Short arms]
OMIM: "Shortening of the arms" [OMIM:Shortening of the arms]
Is a (Direct Parents):
HPO         Aplasia/hypoplasia involving bones of the upper limbs
HPO         Limb undergrowth
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)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Upper limb undergrowth(HPO:0009824)
                   Limb undergrowth(HPO:0009826)
                      Upper limb undergrowth(HPO:0009824)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Upper limb undergrowth(HPO:0009824)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Upper limb undergrowth(HPO:0009824)
                      Limb undergrowth(HPO:0009826)
                         Upper limb undergrowth(HPO:0009824)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
COCOON SYNDROME (OMIM:613630)
DPM1-CDG (Orphanet:79322)
HYDROLETHALUS SYNDROME 1 (OMIM:236680)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
Hydrolethalus (Orphanet:2189)
PELGER-HUET ANOMALY (OMIM:169400)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)