Keratosis pilaris
Symptom Information:
Symptom ID: | MedDRA:10066295 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Hyperkeratoses(MedDRA:10020648) Keratosis pilaris(MedDRA:10066295) |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acromelanosis | (Orphanet:39) |
Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
DERMATITIS, ATOPIC | (OMIM:603165) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
Monilethrix | (Orphanet:573) |
NOONAN SYNDROME 4 | (OMIM:610733) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |