Acromesomelia

Symptom Information:

Symptom ID: HPO:0003086
Synonyms:
Acromesomelia [OMIM:Acromesomelia]
Quality:
Cross references:
OMIM: "Acromesomelia" [OMIM:Acromesomelia]
UMLS:C1864365 "Acromesomelia" [HPO:0003086]
Is a (Direct Parents):
HPO         Mesomelia
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)
                   Limb undergrowth(HPO:0009826)
                      Mesomelia(HPO:0003027)
                         Acromesomelia(HPO:0003086)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Limb undergrowth(HPO:0009826)
                         Mesomelia(HPO:0003027)
                            Acromesomelia(HPO:0003086)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)