FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

56852002: Achromatopsia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
795410010 Achromatopsia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
94543012 Achromatopsia en Synonym Active Case insensitive SNOMED CT core
94544018 Monochromatism en Synonym Active Case insensitive SNOMED CT core
94546016 Achromatism en Synonym Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Achromatopsia Is a Congenital anomaly of retina true Inferred relationship Some
Achromatopsia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Achromatopsia Pathological process Pathological developmental process true Inferred relationship Some 1
Achromatopsia Is a Cone dystrophy true Inferred relationship Some
Achromatopsia Finding site Cone of retina true Inferred relationship Some 1
Achromatopsia Associated morphology Dystrophy true Inferred relationship Some 1
Achromatopsia Is a Developmental hereditary disorder true Inferred relationship Some
Achromatopsia Is a Congenital colour blindness true Inferred relationship Some
Achromatopsia Is a Hereditary retinal dystrophy false Inferred relationship Some
Achromatopsia Is a Hereditary disorder of the visual system false Inferred relationship Some
Achromatopsia Occurrence Congenital false Inferred relationship Some
Achromatopsia Has interpretation Abnormal false Inferred relationship Some 1
Achromatopsia Interprets Vision observable false Inferred relationship Some 1
Achromatopsia Interprets Visual function false Inferred relationship Some 1
Achromatopsia Has interpretation Abnormal false Inferred relationship Some 1
Achromatopsia Interprets Visual function false Inferred relationship Some 1
Achromatopsia Occurrence Congenital true Inferred relationship Some 1
Achromatopsia Finding site Retinal structure false Inferred relationship Some 1
Achromatopsia Associated morphology Dystrophy false Inferred relationship Some 2
Achromatopsia Finding site Retinal structure false Inferred relationship Some 2
Achromatopsia Finding site Retinal structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Complete achromatopsia Is a True Achromatopsia Inferred relationship Some
Incomplete achromatopsia Is a True Achromatopsia Inferred relationship Some
Cone monochromatism Is a False Achromatopsia Inferred relationship Some
Rod monochromatism Is a False Achromatopsia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start