Generalized hyperkeratosis
Symptom Information:
Symptom ID: | HPO:0005595 | ||||||||||||||||||||||||||||||||||
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) Hyperkeratosis(HPO:0000962) Generalized hyperkeratosis(HPO:0005595) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Hyperkeratoses(MedDRA:10020648) Generalized hyperkeratosis(HPO:0005595) |
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Database Frequency: | 14 / 7739 | ||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME | (OMIM:615510) |
Ankylosing vertebral hyperostosis with tylosis | (Orphanet:2206) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Fetal Gaucher disease | (Orphanet:85212) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
Leprechaunism | (Orphanet:508) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Progressive symmetric erythrokeratodermia | (Orphanet:316) |
Transgrediens et progrediens palmoplantar keratoderma | (Orphanet:495) |
Tyrosinemia type 2 | (Orphanet:28378) |
Werner syndrome | (Orphanet:902) |