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2625009: Senter syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5469016 Senter syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
756661011 Senter syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3881187011 Autosomal dominant keratitis, ichthyosis, deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3881188018 Autosomal dominant 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
Senter syndrome Is a Ectodermal dysplasia false Inferred relationship Existential restriction modifier
Senter syndrome Is a Keratitis ichthyosis and deafness syndrome true Inferred relationship Existential restriction modifier
Senter syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Senter syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Senter syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Senter syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Senter syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Senter syndrome Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Senter syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Senter syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Senter syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Senter syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Senter syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Senter syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Senter syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Senter syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Senter syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 3
Senter syndrome Finding site Ectoderm structure false Inferred relationship Existential restriction modifier 3
Senter syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Senter syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Senter syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Senter syndrome Finding site Ectoderm structure true Inferred relationship Existential restriction modifier 1
Senter syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 2
Senter syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 3
Senter syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 3
Senter syndrome Finding site Entire skin true Inferred relationship Existential restriction modifier 2
Senter syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Senter syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 4
Senter syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier 4
Senter syndrome Interprets Hearing, function false Inferred relationship Existential restriction modifier 5
Senter syndrome Is a Autosomal dominant ichthyosis true Inferred relationship Existential restriction modifier
Senter syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Senter syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 4
Senter syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Senter syndrome Finding site Structure of auditory system 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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