FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

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
10063651000172118 syndrome KID (keratitis, ichthyosis, deafness) autosomique récessif fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
10063661000172116 syndrome autosomique récessif de kératite, ichtyose et surdité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4345031000172111 syndroom met autosomaal recessieve keratitis, ichtyosis en doofheid nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4345041000172116 autosomaal recessief keratitis-ichthyosis-doofheid-syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4345051000172119 autosomaal recessief KID-syndroom nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


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 (disorder) true Inferred relationship Some
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Structure of skin region false Inferred relationship Some
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Some
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Hyperkeratosis true Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Interprets Keratinization true Inferred relationship Some 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Has interpretation Abnormal true Inferred relationship Some 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Entire skin true Inferred relationship Some 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site Ectoderm structure true Inferred relationship Some 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Interprets Hearing true Inferred relationship Some 5
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Is a Autosomal recessive ichthyosis (disorder) true Inferred relationship Some
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Has interpretation Decreased true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start