Congenital craniofacial dysostosis

Symptom Information:

Symptom ID: HPO:0008497
Synonyms:
Congenital craniofacial dysostosis [OMIM:Congenital craniofacial dysostosis]
Quality:
Cross references:
OMIM: "Congenital craniofacial dysostosis" [OMIM:Congenital craniofacial dysostosis]
Is a (Direct Parents):
HPO         Craniofacial dysostosis
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)
                   Craniofacial dysostosis(HPO:0004439)
                      Congenital craniofacial dysostosis(HPO:0008497)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Craniofacial dysostosis(HPO:0004439)
                   Congenital craniofacial dysostosis(HPO:0008497)
             Abnormality of the skull(HPO:0000929)
                Craniofacial dysostosis(HPO:0004439)
                   Congenital craniofacial dysostosis(HPO:0008497)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION (OMIM:259660)