Sclerosis of skull base
Symptom Information:
Symptom ID: | HPO:0002694 | ||||||
Synonyms: |
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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 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 skull base(HPO:0002693) Sclerosis of skull base(HPO:0002694) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the skull(HPO:0000929) Abnormality of the skull base(HPO:0002693) Sclerosis of skull base(HPO:0002694) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Camurati-Engelmann disease | (Orphanet:1328) |
Craniometaphyseal dysplasia | (Orphanet:1522) |
Dysosteosclerosis | (Orphanet:1782) |
Greenberg dysplasia | (Orphanet:1426) |
Hurler syndrome | (Orphanet:93473) |
Lateral meningocele syndrome | (Orphanet:2789) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Otopalatodigital syndrome | (Orphanet:669) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |