Brachyturricephaly

Symptom Information:

Symptom ID: HPO:0000244
Synonyms:
Turribrachycephaly [HPO:0000244]
Brachyturricephaly [OMIM:Brachyturricephaly]
Turribrachycephaly [OMIM:Turribrachycephaly]
Quality:
Cross references:
OMIM: "Brachyturricephaly" [OMIM:Brachyturricephaly]
OMIM: "Turribrachycephaly" [OMIM:Turribrachycephaly]
UMLS:C1843494 "Brachyturricephaly" [HPO:0000244]
Is a (Direct Parents):
HPO         Turricephaly
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)
                         Brachyturricephaly(HPO:0000244)
                      Turricephaly(HPO:0000262)
                         Brachyturricephaly(HPO:0000244)
       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)
                            Brachyturricephaly(HPO:0000244)
                         Turricephaly(HPO:0000262)
                            Brachyturricephaly(HPO:0000244)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Apert syndrome (Orphanet:87)
Baller-Gerold syndrome (Orphanet:1225)
Craniofacial dyssynostosis (Orphanet:1516)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Pfeiffer syndrome (Orphanet:710)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Zellweger syndrome (Orphanet:912)