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773635001: Proliferative hyperkeratosis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3725042014 Proliferative hyperkeratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725043016 Proliferative hyperkeratosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proliferative hyperkeratosis Is a Hyperkeratosis true Inferred relationship Some
Proliferative hyperkeratosis Is a Proliferation true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1
Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome is an ectodermal dysplasia syndrome characterized by severe generalized lamellar icthyosis at birth with alopecia, eclabium, ectropion and intellectual disability. Although similar to Sjögren-Larsson syndrome, this syndrome lacks the presence of neurologic or macular changes. There have been no further descriptions in the literature since 1987. Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 3
Lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1
Non-erythrodermic lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may include eye involvement (optic atrophy, diplopia), neuromuscular involvement (ataxia, pyramidal syndrome, gait disturbance) and sensory disorder. There have been no further descriptions in the literature since 1992. Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 2
Lamellar ichthyosis (limited type) (disorder) Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1
Self-healing collodion baby (SHCB) is a minor variant of autosomal recessive congenital ichthyosis characterized by the presence of a collodion membrane at birth that heals within the first weeks of life. Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1
A variant of self-healing collodion baby (SHCB) characterized by the presence at birth of a collodion membrane only at the extremities. Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1
Erythrodermic lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis Inferred relationship Some 1

This concept is not in any reference sets

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