Cranium bifidum occultum

Symptom Information:

Symptom ID: HPO:0004423
Synonyms:
Cranium bifidum occultum [OMIM:Cranium bifidum occultum]
Cranium bifidum occultum (defect in midline frontal bone) [OMIM:Cranium bifidum occultum (defect in midline frontal bone)]
Quality:
Cross references:
OMIM: "Cranium bifidum occultum" [OMIM:Cranium bifidum occultum]
OMIM: "Cranium bifidum occultum (defect in midline frontal bone)" [OMIM:Cranium bifidum occultum (defect in midline frontal bone)]
Is a (Direct Parents):
HPO         Encephalocele
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)
                   Cephalocele(HPO:0011815)
                      Encephalocele(HPO:0002084)
                         Cranium bifidum occultum(HPO:0004423)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Cephalocele(HPO:0011815)
                   Encephalocele(HPO:0002084)
                      Cranium bifidum occultum(HPO:0004423)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia (Orphanet:250)