Perifollicular hyperkeratosis
Symptom Information:
Symptom ID: | HPO:0007468 | ||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Thickened skin(HPO:0001072) Epidermal thickening(HPO:0011368) Hyperkeratosis(HPO:0000962) Perifollicular hyperkeratosis(HPO:0007468) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME | (OMIM:615510) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
Monilethrix | (Orphanet:573) |