Generalized keratosis follicularis
Symptom Information:
Symptom ID: | HPO:0007439 | ||
Synonyms: |
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Cross references: |
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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) Generalized keratosis follicularis(HPO:0007439) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
Keratosis follicularis - dwarfism - cerebral atrophy | (Orphanet:2339) |