Hypoplasia of the frontal bone

Symptom Information:

Symptom ID: HPO:0005466
Synonyms:
Hypoplastic frontal bones [HPO:0005466]
Frontal bone hypoplasia [OMIM:Frontal bone hypoplasia]
Hypoplastic frontal bones [OMIM:Hypoplastic frontal bones]
Quality:
Cross references:
OMIM: "Frontal bone hypoplasia" [OMIM:Frontal bone hypoplasia]
OMIM: "Hypoplastic frontal bones" [OMIM:Hypoplastic frontal bones]
Is a (Direct Parents):
HPO         Abnormal shape of the frontal region
HPO         Hypoplastic facial bones
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)
                         Abnormal shape of the frontal region(HPO:0011218)
                            Hypoplasia of the frontal bone(HPO:0005466)
                   Abnormality of facial skeleton(HPO:0011821)
                      Hypoplastic facial bones(HPO:0002692)
                         Hypoplasia of the frontal bone(HPO:0005466)
       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)
                      Abnormal shape of the frontal region(HPO:0011218)
                         Hypoplasia of the frontal bone(HPO:0005466)
                Abnormality of facial skeleton(HPO:0011821)
                   Hypoplastic facial bones(HPO:0002692)
                      Hypoplasia of the frontal bone(HPO:0005466)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)