Sparse, fine hair
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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Database Frequency: | 4 / 7739 | |
Resource: |
All diseases associated with this symptom:
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Myhre syndrome | (Orphanet:2588) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
Trichodental syndrome | (Orphanet:3351) |