Cranial asymmetry

Symptom Information:

Symptom ID: HPO:0000267
Synonyms:
Cranial asymmetry [OMIM:Cranial asymmetry]
Quality:
Cross references:
OMIM: "Cranial asymmetry" [OMIM:Cranial asymmetry]
Is a (Direct Parents):
HPO         Abnormality of calvarial morphology
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)
                      Cranial asymmetry(HPO:0000267)
       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)
                         Cranial asymmetry(HPO:0000267)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Linear nevus sebaceus syndrome (Orphanet:2612)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Opitz G/BBB syndrome (Orphanet:2745)
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) (OMIM:614886)
Wolf-Hirschhorn syndrome (Orphanet:280)