FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

2625009: Senter syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3881187011 Autosomal dominant keratitis, ichthyosis, deafness syndrome en Synonym Active Case insensitive SNOMED CT core
3881188018 Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome en Synonym Active Initial character case insensitive SNOMED CT core
5469016 Senter syndrome en Synonym Active Case sensitive SNOMED CT core
756661011 Senter syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Senter syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Senter syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Senter syndrome Occurrence Congenital true Inferred relationship Some 1
Senter syndrome Finding site Ectoderm structure true Inferred relationship Some 1
Senter syndrome Associated morphology Hyperkeratosis true Inferred relationship Some 2
Senter syndrome Has interpretation Abnormal true Inferred relationship Some 3
Senter syndrome Interprets Keratinisation true Inferred relationship Some 3
Senter syndrome Finding site Entire skin true Inferred relationship Some 2
Senter syndrome Occurrence Congenital false Inferred relationship Some 4
Senter syndrome Pathological process Pathological developmental process false Inferred relationship Some 4
Senter syndrome Finding site Structure of auditory system false Inferred relationship Some 4
Senter syndrome Interprets Hearing false Inferred relationship Some 5
Senter syndrome Is a Autosomal dominant ichthyosis true Inferred relationship Some
Senter syndrome Interprets Hearing true Inferred relationship Some 4
Senter syndrome Has interpretation Decreased true Inferred relationship Some 4
Senter syndrome Occurrence Congenital true Inferred relationship Some 5
Senter syndrome Finding site Structure of auditory system true Inferred relationship Some 5
Senter syndrome Associated morphology Congenital anomaly false Inferred relationship Some
Senter syndrome Is a Ectodermal dysplasia false Inferred relationship Some
Senter syndrome Is a Keratitis ichthyosis and deafness syndrome true Inferred relationship Some
Senter syndrome Is a Site-specific disorder of skin false Inferred relationship Some
Senter syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Senter syndrome Finding site Skin structure false Inferred relationship Some 1
Senter syndrome Finding site Skin structure false Inferred relationship Some 1
Senter syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Senter syndrome Occurrence Congenital true Inferred relationship Some 2
Senter syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Senter syndrome Finding site Skin structure false Inferred relationship Some 2
Senter syndrome Occurrence Congenital false Inferred relationship Some 3
Senter syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 3
Senter syndrome Finding site Ectoderm structure false Inferred relationship Some 3
Senter syndrome Occurrence Congenital false Inferred relationship Some
Senter syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Senter syndrome Finding site Structure of skin region false Inferred relationship Some 1
Senter syndrome Finding site Skin structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start