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110445001: Focal hyperkeratosis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
175279019 Focal hyperkeratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
175280016 Focal keratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622251012 Focal hyperkeratosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6990191000241116 hyperkératose focale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Focal hyperkeratosis Is a Growth alteration false Inferred relationship Some
Focal hyperkeratosis Is a Hyperkeratosis true Inferred relationship Some
Focal hyperkeratosis Is a Lesion (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Subungual corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Soft corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Corn of toe Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Hard corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Corn - lesion Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Neurovascular corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Interdigital corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Intractable plantar keratoma Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Vascular corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Seed corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Durlachers corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Corns NOS Associated morphology False Focal hyperkeratosis Inferred relationship Some 1
Intractable plantar keratoma Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Interdigital corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Fibrous corn (disorder) Associated morphology False Focal hyperkeratosis Inferred relationship Some 4
Soft corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Hard corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Corn - lesion Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Neurovascular corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Vascular corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Seed corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Durlachers corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 3
Subungual corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 4
Corn of toe Associated morphology False Focal hyperkeratosis Inferred relationship Some 4
Interdigital corn Associated morphology False Focal hyperkeratosis Inferred relationship Some 3
Intractable plantar keratoma Associated morphology False Focal hyperkeratosis Inferred relationship Some 3
Fibrous corn (disorder) Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Striate palmoplantar keratoderma is an isolated, focal, hereditary palmoplantar keratoderma characterized by linear hyperkeratosis along the flexor aspect of the fingers and on palms, as well as focal hyperkeratosis of the plantar skin. Patients present with painful thickening of the skin on palms and soles, with occasional fissuring, blistering and hyperhidrosis. Rarely, hyperkeratosis on other areas may be seen (knees, dorsal aspects of the digits). Histopathologically, widened intercellular spaces between keratinocytes are observed. Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Focal palmoplantar and gingival keratoderma is a very rare form of focal palmoplantar keratoderma characterized by painful circumscribed hyperkeratotic lesions on weight-bearing areas of soles, moderate focal hyperkeratosis of palmar pressure-related areas and an asymptomatic leukokeratosis confined to labial- and lingual- attached gingiva. Additional occasional features may include hyperhidrosis, follicular keratosis and extended oral mucosa involvement. Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
Intractable plantar keratoma Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Focal acral hyperkeratosis (disorder) Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
Focal acral hyperkeratosis (disorder) Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Focal palmoplantar and gingival keratoderma is a very rare form of focal palmoplantar keratoderma characterized by painful circumscribed hyperkeratotic lesions on weight-bearing areas of soles, moderate focal hyperkeratosis of palmar pressure-related areas and an asymptomatic leukokeratosis confined to labial- and lingual- attached gingiva. Additional occasional features may include hyperhidrosis, follicular keratosis and extended oral mucosa involvement. Associated morphology False Focal hyperkeratosis Inferred relationship Some 3
Circumscribed palmoplantar keratoderma Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Circumscribed palmoplantar keratoderma Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
Keratoderma areata Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Keratoderma areata Associated morphology False Focal hyperkeratosis Inferred relationship Some 3
Keratoderma with pachyonychia congenita Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Keratoderma with pachyonychia congenita Associated morphology False Focal hyperkeratosis Inferred relationship Some 3
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) Associated morphology False Focal hyperkeratosis Inferred relationship Some 2
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) Associated morphology False Focal hyperkeratosis Inferred relationship Some 3
Keratoderma climactericum Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Subungual corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Interdigital corn Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Focal palmoplantar and gingival keratoderma is a very rare form of focal palmoplantar keratoderma characterized by painful circumscribed hyperkeratotic lesions on weight-bearing areas of soles, moderate focal hyperkeratosis of palmar pressure-related areas and an asymptomatic leukokeratosis confined to labial- and lingual- attached gingiva. Additional occasional features may include hyperhidrosis, follicular keratosis and extended oral mucosa involvement. Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
Striate palmoplantar keratoderma is an isolated, focal, hereditary palmoplantar keratoderma characterized by linear hyperkeratosis along the flexor aspect of the fingers and on palms, as well as focal hyperkeratosis of the plantar skin. Patients present with painful thickening of the skin on palms and soles, with occasional fissuring, blistering and hyperhidrosis. Rarely, hyperkeratosis on other areas may be seen (knees, dorsal aspects of the digits). Histopathologically, widened intercellular spaces between keratinocytes are observed. Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
A rare genetic skin disease characterized by generalized skin peeling or superficial blisters without scarring, leukonychia, acral punctate keratoses coalescing into focal keratoderma on the weight-bearing areas, painful angular cheilitis, and knuckle pads with multiple hyperkeratotic micropapules. The skin appears dry and scaly with superficial exfoliation and underlying erythema. Histopathologic examination of affected skin areas is not specific and shows hyperkeratosis, acanthosis, and occasional intraepidermal clefting with irregular acantholysis. Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
A rare genetic skin disease characterized by generalized skin peeling or superficial blisters without scarring, leukonychia, acral punctate keratoses coalescing into focal keratoderma on the weight-bearing areas, painful angular cheilitis, and knuckle pads with multiple hyperkeratotic micropapules. The skin appears dry and scaly with superficial exfoliation and underlying erythema. Histopathologic examination of affected skin areas is not specific and shows hyperkeratosis, acanthosis, and occasional intraepidermal clefting with irregular acantholysis. Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
A rare hereditary palmoplantar keratoderma characterized by focal hyperkeratotic lesions on the palms and soles. Histopathologic examination reveals prominent hyperkeratosis, thickened stratum spinosum with reduced stratum granulosum, disadhesion of cells in the suprabasal layers, elongation of rete ridges, and sparse lymphocyte infiltration in the dermis. Associated morphology True Focal hyperkeratosis Inferred relationship Some 1
A rare hereditary palmoplantar keratoderma characterized by focal hyperkeratotic lesions on the palms and soles. Histopathologic examination reveals prominent hyperkeratosis, thickened stratum spinosum with reduced stratum granulosum, disadhesion of cells in the suprabasal layers, elongation of rete ridges, and sparse lymphocyte infiltration in the dermis. Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
A rare genetic disease characterised by thickening of the skin on palms and soles restricted to areas of weight bearing and/or friction (focal, non-epidermolytic palmoplantar keratoderma) and oral and oesophageal leucokeratosis, associated with a very high lifetime risk of developing squamous cell carcinoma of the oesophagus. The skin lesions appear in childhood and can be complicated by fissuring and infection. Associated morphology True Focal hyperkeratosis Inferred relationship Some 2
A rare genetic disease characterised by thickening of the skin on palms and soles restricted to areas of weight bearing and/or friction (focal, non-epidermolytic palmoplantar keratoderma) and oral and oesophageal leucokeratosis, associated with a very high lifetime risk of developing squamous cell carcinoma of the oesophagus. The skin lesions appear in childhood and can be complicated by fissuring and infection. Associated morphology True Focal hyperkeratosis Inferred relationship Some 1

This concept is not in any reference sets

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