FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

28835009: Retinitis pigmentosa (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
48282015 Retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
759560017 Retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1226074019 RP - Retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
48282015 Retinitis pigmentosa en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
48282015 Retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
759560017 Retinitis pigmentosa (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
759560017 Retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1226074019 RP - Retinitis pigmentosa en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1226074019 RP - Retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
949071000195116 retinite pigmentosa it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427871001000115 Retinitis pigmentosa de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
614231000172113 rétinite pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
614231000172113 rétinite pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
949071000195116 retinite pigmentosa it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427871001000115 Retinitis pigmentosa de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


31 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa (disorder) Is a Hereditary retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa (disorder) Is a Autosomal hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa (disorder) Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinitis pigmentosa (disorder) Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant retinitis pigmentosa Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive retinitis pigmentosa Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked retinitis pigmentosa Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked retinitis pigmentosa heterozygote (disorder) Is a False Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa-deafness syndrome (disorder) Is a False Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tapetoretinal dystrophy Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Phytanic acid storage disease (disorder) Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of retinitis pigmentosa (situation) Associated finding True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a False Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Oculotrichodysplasia Is a False Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) Is a False Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
History of retinitis pigmentosa Associated finding True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinitis pigmentosa due to systemic disease (disorder) Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder) Is a True Retinitis pigmentosa (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start