Autosomal dominant contiguous gene syndrome
Symptom Information:
Symptom ID: | HPO:0001452 | ||||
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Mode of inheritance(HPO:0000005) Autosomal dominant inheritance(HPO:0000006) Autosomal dominant contiguous gene syndrome(HPO:0001452) Contiguous gene syndrome(HPO:0001466) Autosomal dominant contiguous gene syndrome(HPO:0001452) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME | (OMIM:600257) |
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality | (Orphanet:86841) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
Waardenburg syndrome | (Orphanet:3440) |