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70041004: Erythrokeratodermia variabilis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
116327014 Erythrokeratodermia variabilis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810054016 Erythrokeratodermia variabilis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1233217010 Congenital poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1233218017 Mendes da Costa syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
871211000172115 erythrokératodermie variable fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
921491000172116 EKV - erythrokératodermie variable fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrokeratodermia variabilis Is a Skin lesion false Inferred relationship Some
Erythrokeratodermia variabilis Is a Erythrokeratoderma false Inferred relationship Some
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Occurrence Congenital false Inferred relationship Some
Erythrokeratodermia variabilis Associated morphology Hyperkeratosis true Inferred relationship Some 1
Erythrokeratodermia variabilis Associated morphology anomalie congénitale false Inferred relationship Some 2
Erythrokeratodermia variabilis Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Occurrence Congenital false Inferred relationship Some 3
Erythrokeratodermia variabilis Associated morphology anomalie du développement false Inferred relationship Some 3
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 3
Erythrokeratodermia variabilis Is a Disorder of skin (disorder) false Inferred relationship Some
Erythrokeratodermia variabilis Has interpretation Abnormal true Inferred relationship Some 2
Erythrokeratodermia variabilis Interprets Keratinization true Inferred relationship Some 2
Erythrokeratodermia variabilis Is a Ichthyosis false Inferred relationship Some
Erythrokeratodermia variabilis Finding site Entire skin true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Congenital keratoderma true Inferred relationship Some
Erythrokeratodermia variabilis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Congenital anomaly of skin false Inferred relationship Some
Erythrokeratodermia variabilis Occurrence Congenital true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Developmental hereditary disorder false Inferred relationship Some
Erythrokeratodermia variabilis Is a Autosomal hereditary disorder true Inferred relationship Some
Erythrokeratodermia variabilis Is a Congenital ichthyosis of skin true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Malignant atrophic papulosis Is a False Erythrokeratodermia variabilis Inferred relationship Some
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder) Is a False Erythrokeratodermia variabilis Inferred relationship Some
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) Is a False Erythrokeratodermia variabilis Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) Is a False Erythrokeratodermia variabilis Inferred relationship Some

This concept is not in any reference sets

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