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

276436007: Hereditary macular dystrophy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2791808017 Macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
412569012 Hereditary macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
669351013 Hereditary macular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


15 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary macular dystrophy est un(e) (attribut) Degenerative disorder of macula (disorder) true Inferred relationship Some
Hereditary macular dystrophy est un(e) (attribut) Disorder of macula of retina (disorder) false Inferred relationship Some
Hereditary macular dystrophy est un(e) (attribut) Hereditary retinal dystrophy true Inferred relationship Some
Hereditary macular dystrophy morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Hereditary macular dystrophy localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some 1
Hereditary macular dystrophy localisation d'une constatation (attribut) Macula lutea structure false Inferred relationship Some
Hereditary macular dystrophy est un(e) (attribut) Macular dystrophy false Inferred relationship Some
Hereditary macular dystrophy localisation d'une constatation (attribut) Macula lutea structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Martinique crinkled retinal pigment epitheliopathy est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Sorsby's fundus dystrophy est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Dominant drusen est un(e) (attribut) False Hereditary macular dystrophy Inferred relationship Some
Vitelliform dystrophy est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
North Carolina macular dystrophy est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Fundus flavimaculatus (disorder) est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Stargardt's disease est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Other Bruch's membrane dystrophy est un(e) (attribut) False Hereditary macular dystrophy Inferred relationship Some
Bull's eye macular dystrophy est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Pattern dystrophy of macula est un(e) (attribut) False Hereditary macular dystrophy Inferred relationship Some
dystrophie maculaire annulaire concentrique bénigne est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Retinal macular dystrophy type 2 est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some
Occult macular dystrophy (disorder) est un(e) (attribut) True Hereditary macular dystrophy Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start