Aplasia/hypoplasia involving the skeleton

Symptom Information:

Symptom ID: HPO:0009115
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of skeletal morphology
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)