Pigmentary abnormalities
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Coats plus syndrome | (Orphanet:313838) |
Immunodeficiency by defective expression of HLA class 1 | (Orphanet:34592) |
Koolen-De Vries syndrome | (Orphanet:96169) |