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403780007: Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771706016 Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782790010 Autosomal recessive keratitis-ichthyosis-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1787870017 Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771706016 Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771706016 Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782790010 Autosomal recessive keratitis-ichthyosis-deafness syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782790010 Autosomal recessive keratitis-ichthyosis-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1787870017 Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5815381000241115 syndrome KID (keratitis, ichthyosis, deafness) autosomique récessif fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815391000241118 syndrome autosomique récessif de kératite, ichtyose et surdité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815381000241115 syndrome KID (keratitis, ichthyosis, deafness) autosomique récessif fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815391000241118 syndrome autosomique récessif de kératite, ichtyose et surdité 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
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Is a Keratitis ichthyosis and deafness syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Interprets Keratinisation true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Entire skin true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Ectoderm structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 5
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Is a Autosomal recessive ichthyosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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