FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

789676005: Blue cone monochromatism (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3791525013 Blue cone monochromatism en Synonym Active Case insensitive SNOMED CT core
3791529019 Cone monochromatism en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start