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767498008: Autosomal recessive congenital methemoglobinemia type II (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
3672028014 Autosomal recessive congenital methaemoglobinaemia type II en Synonym Active Only initial character case insensitive SNOMED CT core module
3672029018 Autosomal recessive congenital methemoglobinemia type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3672030011 Autosomal recessive congenital methemoglobinemia type II 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 II Is a Autosomal recessive congenital methemoglobinemia true Inferred relationship Existential restriction modifier
Autosomal recessive congenital methemoglobinemia type II Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal recessive congenital methemoglobinemia type II 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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