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28835009: Retinitis pigmentosa (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1226074019 RP - Retinitis pigmentosa en Synonym Active Case sensitive SNOMED CT core
48282015 Retinitis pigmentosa en Synonym Active Case insensitive SNOMED CT core
759560017 Retinitis pigmentosa (disorder) en Fully specified name Active Case insensitive SNOMED CT core


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 Associated morphology Dystrophy true Inferred relationship Some 1
Retinitis pigmentosa Finding site Retinal structure true Inferred relationship Some 1
Retinitis pigmentosa Finding site Retinal structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a True Retinitis pigmentosa Inferred relationship Some
H/O: 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
Retinitis pigmentosa-deafness syndrome Is a False Retinitis pigmentosa Inferred relationship Some
Phytanic acid storage disease Is a True Retinitis pigmentosa Inferred relationship Some
Tapetoretinal dystrophy Is a True Retinitis pigmentosa Inferred relationship Some
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
Family history of retinitis pigmentosa Associated finding True Retinitis pigmentosa Inferred relationship Some 1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome Is a False Retinitis pigmentosa Inferred relationship Some
Oculotrichodysplasia Is a False Retinitis pigmentosa Inferred relationship Some
RHYNS syndrome Is a False Retinitis pigmentosa Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a True Retinitis pigmentosa Inferred relationship Some

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

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