FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  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
614231000172113 rétinite pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


30 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa Is a Hereditary retinal dystrophy true Inferred relationship Some
Retinitis pigmentosa Is a Autosomal hereditary disorder false Inferred relationship Some
Retinitis pigmentosa Finding site Retinal structure false Inferred relationship Some
Retinitis pigmentosa Associated morphology Dystrophy true Inferred relationship Some 1
Retinitis pigmentosa Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant retinitis pigmentosa Is a True Retinitis pigmentosa Inferred relationship Some
Autosomal recessive retinitis pigmentosa Is a True Retinitis pigmentosa Inferred relationship Some
X-linked retinitis pigmentosa Is a True Retinitis pigmentosa Inferred relationship Some
X-linked retinitis pigmentosa heterozygote Is a False Retinitis pigmentosa Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Is a False Retinitis pigmentosa Inferred relationship Some
Tapetoretinal dystrophy Is a True Retinitis pigmentosa Inferred relationship Some
HSMN IV Is a True Retinitis pigmentosa Inferred relationship Some
Family history of retinitis pigmentosa (situation) Associated finding True Retinitis pigmentosa Inferred relationship Some 1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Is a False Retinitis pigmentosa Inferred relationship Some
Oculotrichodysplasia (disorder) Is a False Retinitis pigmentosa Inferred relationship Some
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) Is a False Retinitis pigmentosa Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a True Retinitis pigmentosa Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) Is a True Retinitis pigmentosa Inferred relationship Some
History of retinitis pigmentosa Associated finding True Retinitis pigmentosa Inferred relationship Some 1
Retinitis pigmentosa due to systemic disease Is a True Retinitis pigmentosa Inferred relationship Some

Reference Sets

GB English

US English

Back to Start