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1237228009: Night blindness, skeletal anomalies, dysmorphism syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Aug 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5091257017 Night blindness, skeletal anomalies, dysmorphism syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5091258010 Night blindness, skeletal anomalies, dysmorphism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5091259019 Hunter Thompson Reed syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Night blindness, skeletal anomalies, dysmorphism syndrome Is a Chronic disease of musculoskeletal system true Inferred relationship Existential restriction modifier
Night blindness, skeletal anomalies, dysmorphism syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Night blindness, skeletal anomalies, dysmorphism syndrome Is a Night blindness true Inferred relationship Existential restriction modifier
Night blindness, skeletal anomalies, dysmorphism syndrome Is a Congenital anomaly of musculoskeletal system true Inferred relationship Existential restriction modifier
Night blindness, skeletal anomalies, dysmorphism syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier
Night blindness, skeletal anomalies, dysmorphism syndrome Is a Disorder of skeletal system true Inferred relationship Existential restriction modifier
Night blindness, skeletal anomalies, dysmorphism syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Night blindness, skeletal anomalies, dysmorphism syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 4
Night blindness, skeletal anomalies, dysmorphism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Night blindness, skeletal anomalies, dysmorphism syndrome Finding site Skeletal system structure true Inferred relationship Existential restriction modifier 1
Night blindness, skeletal anomalies, dysmorphism syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Night blindness, skeletal anomalies, dysmorphism syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Night blindness, skeletal anomalies, dysmorphism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Night blindness, skeletal anomalies, dysmorphism syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Night blindness, skeletal anomalies, dysmorphism syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Night blindness, skeletal anomalies, dysmorphism syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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