Calvarial skull defect

Symptom Information:

Symptom ID: HPO:0001362
Synonyms:
Calvarial defect [Orphanet:2600]
Scalp/skull defect [Orphanet:2600]
Quality:
Cross references:
Orphanet:2600 "Scalp/skull defect" [Orphanet:2600]
Is a (Direct Parents):
HPO         Abnormality of calvarial morphology
Orphanet Abnormality of the skull
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)
                      Calvarial skull defect(HPO:0001362)
       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)
                         Calvarial skull defect(HPO:0001362)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Acalvaria (Orphanet:945)
Adams-Oliver syndrome (Orphanet:974)
Aplasia cutis - myopia (Orphanet:1117)
Aplasia cutis congenita - intestinal lymphangiectasia (Orphanet:1116)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIACUTIS CONGENITA (OMIM:302803)
Circumscribed cutaneous aplasia of the vertex (Orphanet:1114)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Fraser syndrome (Orphanet:2052)
Frontal encephalocele (Orphanet:1931)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Greenberg dysplasia (Orphanet:1426)
Johanson-Blizzard syndrome (Orphanet:2315)
Knobloch syndrome (Orphanet:1571)
Methimazole embryofetopathy (Orphanet:1923)
Monosomy 9p (Orphanet:261112)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Phocomelia, Schinzel type (Orphanet:2879)
Primary hypergonadotropic hypogonadism - partial alopecia (Orphanet:2232)
Scalp defects - postaxial polydactyly (Orphanet:1003)
Short rib-polydactyly syndrome (Orphanet:1505)
Trisomy 13 (Orphanet:3378)
Wolf-Hirschhorn syndrome (Orphanet:280)