Somatic mosaicism
Symptom Information:
Symptom ID: | HPO:0001442 | ||
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) Mode of inheritance(HPO:0000005) Somatic mutation(HPO:0001428) Somatic mosaicism(HPO:0001442) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Fibrous dysplasia of bone | (Orphanet:249) |
Ito hypomelanosis | (Orphanet:435) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
SLC35A2-CDG | (Orphanet:356961) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Tetrasomy 12p | (Orphanet:884) |