FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

733522005: Megalocornea with intellectual disability syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3499604011 Megalocornea with intellectual disability syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3499605012 Megalocornea with intellectual disability syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3499606013 MMR (megalocornea, mental retardation) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499607016 Neuhäuser syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403819015 Megalocornea-intellectual disability syndrome is a rare intellectual disability syndrome most commonly characterized by megalocornea, congenital hypotonia, varying degrees of intellectual disability, psychomotor/developmental delay, seizures, and mild facial dysmorphism (including round face, frontal bossing, epicanthal folds, large low set ears, broad nasal base, anteverted nostrils, and long upper lip). Interfamilial and intrafamilial clinical variability has been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403820014 Megalocornea-intellectual disability syndrome is a rare intellectual disability syndrome most commonly characterised by megalocornea, congenital hypotonia, varying degrees of intellectual disability, psychomotor/developmental delay, seizures, and mild facial dysmorphism (including round face, frontal bossing, epicanthal folds, large low set ears, broad nasal base, anteverted nostrils, and long upper lip). Interfamilial and intrafamilial clinical variability has been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Megalocornea with intellectual disability syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
Megalocornea with intellectual disability syndrome Is a Mental retardation false Inferred relationship Some
Megalocornea with intellectual disability syndrome Is a Megalocornea true Inferred relationship Some
Megalocornea with intellectual disability syndrome Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Megalocornea with intellectual disability syndrome Associated morphology Congenital enlargement false Inferred relationship Some 1
Megalocornea with intellectual disability syndrome Occurrence Congenital true Inferred relationship Some 1
Megalocornea with intellectual disability syndrome Finding site Corneal structure true Inferred relationship Some 1
Megalocornea with intellectual disability syndrome Is a Intellectual disability true Inferred relationship Some
Megalocornea with intellectual disability syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Megalocornea with intellectual disability syndrome Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 1
Megalocornea with intellectual disability syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Megalocornea with intellectual disability syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 2
Megalocornea with intellectual disability syndrome Has interpretation Impaired true Inferred relationship Some 2
Megalocornea with intellectual disability syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 3
Megalocornea with intellectual disability syndrome Has interpretation Impaired true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start