Calvarial skull defect
Symptom Information:
Symptom ID: | HPO:0001362 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |