FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

763067000: Autosomal dominant congenital benign spinal muscular atrophy (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
3637758012 Autosomal dominant congenital benign spinal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
3637759016 Autosomal dominant congenital benign spinal muscular atrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3637760014 Autosomal dominant benign distal spinal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
3637761013 Congenital benign spinal muscular atrophy with contracture en Synonym Active Entire term case insensitive SNOMED CT core module
3637762018 Congenital nonprogressive spinal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant congenital benign spinal muscular atrophy Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal dominant congenital benign spinal muscular atrophy Is a Congenital disease true Inferred relationship Existential restriction modifier
Autosomal dominant congenital benign spinal muscular atrophy Is a Distal spinal muscular atrophy true Inferred relationship Existential restriction modifier
Autosomal dominant congenital benign spinal muscular atrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital benign spinal muscular atrophy Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital benign spinal muscular atrophy Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant congenital benign spinal muscular atrophy Finding site Nerve structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant congenital benign spinal muscular atrophy Is a Autosomal dominant distal hereditary motor neuropathy true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start