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73663008: Disorder of central nervous system due to xeroderma pigmentosum (disorder)

Status: current, 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
122320010 Neurologic xeroderma pigmentosum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2548038016 Disorder of central nervous system due to xeroderma pigmentosum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5248010015 Disorder of central nervous system due to xeroderma pigmentosum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
122320010 Neurologic xeroderma pigmentosum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
122320010 Neurologic xeroderma pigmentosum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
122320010 Neurologic xeroderma pigmentosum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
814076017 Neurologic xeroderma pigmentosum (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
814076017 Neurologic xeroderma pigmentosum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2532596019 Disorder of central nerous system due to xeroderma pigmentosum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2548038016 Disorder of central nervous system due to xeroderma pigmentosum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2548038016 Disorder of central nervous system due to xeroderma pigmentosum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5248010015 Disorder of central nervous system due to xeroderma pigmentosum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4631091000241112 xeroderma pigmentosum neurologique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4631091000241112 xeroderma pigmentosum neurologique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Is a Xeroderma pigmentosum (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Is a Disorder of skin AND/OR subcutaneous tissue of head (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Is a retard mental false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Associated morphology Atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 4
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Associated morphology Papulovesicular rash false Inferred relationship Existential restriction modifier (core metadata concept) 3
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Is a Disorder of the central nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Due to Xeroderma pigmentosum (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa Is a False Disorder of central nervous system due to xeroderma pigmentosum (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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