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767499000: Autosomal recessive congenital methemoglobinemia type I (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3672031010 Autosomal recessive congenital methemoglobinemia type I en Synonym Active Only initial character case insensitive SNOMED CT core module
3672032015 Autosomal recessive congenital methemoglobinemia type I (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3672033013 Autosomal recessive congenital methaemoglobinaemia type I en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive congenital methemoglobinemia type I Is a Autosomal recessive congenital methemoglobinemia true Inferred relationship Existential restriction modifier
Autosomal recessive congenital methemoglobinemia type I Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital methemoglobinemia type I Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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