Acrobrachycephaly

Symptom Information:

Symptom ID: HPO:0004487
Synonyms:
Acrobrachycephaly [OMIM:Acrobrachycephaly]
Quality:
Cross references:
OMIM: "Acrobrachycephaly" [OMIM:Acrobrachycephaly]
UMLS:C1863395 "Acrobrachycephaly" [HPO:0004487]
Is a (Direct Parents):
HPO         Brachycephaly
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the calvaria(HPO:0002683)
                   Abnormality of calvarial morphology(HPO:0002648)
                      Brachycephaly(HPO:0000248)
                         Acrobrachycephaly(HPO:0004487)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the calvaria(HPO:0002683)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Brachycephaly(HPO:0000248)
                            Acrobrachycephaly(HPO:0004487)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Apert syndrome (Orphanet:87)