Keratosis follicular
Symptom Information:
| Symptom ID: | MedDRA:10023369 | ||
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HPO:
MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Skin and subcutaneous tissue disorders congenital(MedDRA:10040789) Skin and subcutaneous tissue disorders congenital NEC(MedDRA:10040834) Keratosis follicular(MedDRA:10023369) |
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| Database Frequency: | 5 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
| Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
| KYRLE DISEASE | (OMIM:149500) |
| Monilethrix | (Orphanet:573) |
| Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |