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


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

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 SNOMED CT core module
1782790010 Autosomal recessive keratitis-ichthyosis-deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1787870017 Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive keratitis-ichthyosis-deafness syndrome Is a Keratitis ichthyosis and deafness syndrome true Inferred relationship Existential restriction modifier
Autosomal recessive keratitis-ichthyosis-deafness syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier
Autosomal recessive keratitis-ichthyosis-deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Entire skin true Inferred relationship Existential restriction modifier 1
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Autosomal recessive keratitis-ichthyosis-deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome Finding site Ectoderm structure true Inferred relationship Existential restriction modifier 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 5
Autosomal recessive keratitis-ichthyosis-deafness syndrome Is a Autosomal recessive ichthyosis true Inferred relationship Existential restriction modifier
Autosomal recessive keratitis-ichthyosis-deafness syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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