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776087007: Autosomal recessive cerebral atrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3736330010 Autosomal recessive cerebral atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
3736331014 Autosomal recessive cerebral atrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive cerebral atrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive cerebral atrophy Associated morphology Atrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebral atrophy Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Autosomal recessive cerebral atrophy Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebral atrophy Is a Cerebral atrophy true Inferred relationship Existential restriction modifier
Autosomal recessive cerebral atrophy Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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