Oxycephaly

Symptom Information:

Symptom ID: HPO:0000263
Synonyms:
Acrocephaly [HPO:0000263]
Acrocephaly [OMIM:Acrocephaly]
Oxycephaly [OMIM:Oxycephaly]
Acrocephaly (rare) [OMIM:Acrocephaly (rare)]
Quality:
Cross references:
OMIM: "Acrocephaly" [OMIM:Acrocephaly]
OMIM: "Oxycephaly" [OMIM:Oxycephaly]
OMIM: "Acrocephaly (rare)" [OMIM:Acrocephaly (rare)]
UMLS:C0030044 "Acrocephaly" [HPO:0000263]
Is a (Direct Parents):
HPO         Turricephaly
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)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the calvaria(HPO:0002683)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Turricephaly(HPO:0000262)
                            Oxycephaly(HPO:0000263)
       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)
                      Turricephaly(HPO:0000262)
                         Oxycephaly(HPO:0000263)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Acrocephalopolydactyly (Orphanet:221054)
Acrocraniofacial dysostosis (Orphanet:949)
CARPENTER SYNDROME 2 (OMIM:614976)
Craniorhiny (Orphanet:157832)
Goodman syndrome (Orphanet:65798)
Isolated oxycephaly (Orphanet:63440)
Isolated scaphocephaly (Orphanet:35093)
Saethre-Chotzen syndrome (Orphanet:794)
Sakati-Nyhan syndrome (Orphanet:3128)
Summitt syndrome (Orphanet:3210)