Aplasia/hypoplasia involving the skeleton
Symptom Information:
Symptom ID: | HPO:0009115 | ||
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) MedDRA: |
||
Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
CHILD syndrome | (Orphanet:139) |
Campomelic dysplasia | (Orphanet:140) |
Circumscribed cutaneous aplasia of the vertex | (Orphanet:1114) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Treacher-Collins syndrome | (Orphanet:861) |