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789676005: Blue cone monochromatism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3791524012 Blue cone monochromatism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3791525013 Blue cone monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3791529019 Cone monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Blue cone monochromatism (disorder) Is a Congenital anomaly of retina true Inferred relationship Some
Blue cone monochromatism (disorder) Is a Cone dystrophy true Inferred relationship Some
Blue cone monochromatism (disorder) Occurrence Congenital true Inferred relationship Some 1
Blue cone monochromatism (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Blue cone monochromatism (disorder) Is a Congenital color blindness true Inferred relationship Some
Blue cone monochromatism (disorder) Is a X-linked hereditary disease false Inferred relationship Some
Blue cone monochromatism (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Blue cone monochromatism (disorder) Finding site Cone of retina true Inferred relationship Some 1
Blue cone monochromatism (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Blue cone monochromatism (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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