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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
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 (morphologic abnormality) Is a Hyperkeratosis true Inferred relationship Existential restriction modifier (core metadata concept)
Proliferative hyperkeratosis (morphologic abnormality) Is a Proliferation true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant lamellar ichthyosis (disorder) Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome is an ectodermal dysplasia syndrome characterised by severe generalised 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 (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-erythrodermic lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 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 (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Lamellar ichthyosis (limited type) (disorder) Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Self-healing collodion baby Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acral self-healing collodion baby Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrodermic lamellar ichthyosis Associated morphology True Proliferative hyperkeratosis (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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