Acromesomelia
Symptom Information:
Symptom ID: | HPO:0003086 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |