FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

722458000: Matthew Wood syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3332221010 Anophthalmia with pulmonary hypoplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3332222015 Matthew Wood syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3332223013 Syndromic microphthalmia type 9 en Synonym Active Entire term case insensitive SNOMED CT core module
3332225018 Matthew Wood syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Matthew Wood syndrome Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Matthew Wood syndrome Is a Congenital anomaly of eye true Inferred relationship Existential restriction modifier
Matthew Wood syndrome Is a Congenital anomaly of lung true Inferred relationship Existential restriction modifier
Matthew Wood syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Matthew Wood syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Matthew Wood syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Matthew Wood syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Matthew Wood syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Matthew Wood syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Matthew Wood syndrome Finding site Lung structure true Inferred relationship Existential restriction modifier 2
Matthew Wood syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 3
Matthew Wood syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Matthew Wood syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Matthew Wood syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Matthew Wood syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Matthew Wood syndrome Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 1
Matthew Wood syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Matthew Wood syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start