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28835009: Retinitis pigmentosa (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
48282015 Retinitis pigmentosa en Synonym Active Entire term case insensitive SNOMED CT core module
759560017 Retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1226074019 RP - Retinitis pigmentosa en Synonym Active Entire term case sensitive SNOMED CT core 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 Existential restriction modifier
Retinitis pigmentosa Is a Autosomal hereditary disorder false Inferred relationship Existential restriction modifier
Retinitis pigmentosa Finding site Retinal structure false Inferred relationship Existential restriction modifier
Retinitis pigmentosa Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa Finding site Retinal structure true Inferred relationship Existential restriction modifier 1

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

This concept is not in any reference sets

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