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

733604003: Microcephalus, lymphedema, chorioretinopathy syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3500036015 Microcephalus, lymphedema, chorioretinopathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3500037012 Microcephalus, lymphedema, chorioretinopathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3500040012 MLCRD (microcephaly with or without chorioretinopathy, lymphoedema or intellectual disability) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3500041011 MLCRD (microcephaly with or without chorioretinopathy, lymphedema or intellectual disability) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3500042016 Microcephalus, lymphoedema, chorioretinopathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Microcephalus false Inferred relationship Existential restriction modifier
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Microcephalus, lymphedema, chorioretinopathy syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 1
Microcephalus, lymphedema, chorioretinopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microcephalus, lymphedema, chorioretinopathy syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 1
Microcephalus, lymphedema, chorioretinopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Microcephalus, lymphedema, chorioretinopathy syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Microcephalus, lymphedema, chorioretinopathy syndrome Finding site Head structure true Inferred relationship Existential restriction modifier 1
Microcephalus, lymphedema, chorioretinopathy syndrome Interprets Birth head circumference true Inferred relationship Existential restriction modifier 2
Microcephalus, lymphedema, chorioretinopathy syndrome Is a Congenital microcephaly 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