FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

732951005: Mitochondrial myopathy, lactic acidosis, deafness syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3498427016 Mitochondrial myopathy, lactic acidosis, deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3498428014 Mitochondrial myopathy, lactic acidosis, hearing loss syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3498429018 Mitochondrial myopathy, lactic acidosis, deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3499918019 A type of metabolic myopathy described only in two sisters to date, presenting during childhood, and characterised clinically by growth failure, severe muscle weakness, and moderate sensorineural deafness and biochemically by metabolic acidosis, elevated serum pyruvate concentration, hyperalaninaemia and hyperalaninuria. There have been no further descriptions in the literature since 1973. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499919010 A type of metabolic myopathy described only in two sisters to date, presenting during childhood, and characterized clinically by growth failure, severe muscle weakness, and moderate sensorineural deafness and biochemically by metabolic acidosis, elevated serum pyruvate concentration, hyperalaninemia and hyperalaninuria. There have been no further descriptions in the literature since 1973. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mitochondrial myopathy, lactic acidosis, deafness syndrome Is a Mitochondrial myopathy true Inferred relationship Some
Mitochondrial myopathy, lactic acidosis, deafness syndrome Is a Sensorineural hearing loss true Inferred relationship Some
Mitochondrial myopathy, lactic acidosis, deafness syndrome Is a Lactic acidosis true Inferred relationship Some
Mitochondrial myopathy, lactic acidosis, deafness syndrome Is a Congenital hearing disorder false Inferred relationship Some
Mitochondrial myopathy, lactic acidosis, deafness syndrome Is a Hearing loss associated with syndrome true Inferred relationship Some
Mitochondrial myopathy, lactic acidosis, deafness syndrome Finding site Ear structure false Inferred relationship Some 2
Mitochondrial myopathy, lactic acidosis, deafness syndrome Interprets Hearing false Inferred relationship Some 3
Mitochondrial myopathy, lactic acidosis, deafness syndrome Interprets Functional observable false Inferred relationship Some
Mitochondrial myopathy, lactic acidosis, deafness syndrome Occurrence Congenital false Inferred relationship Some 4
Mitochondrial myopathy, lactic acidosis, deafness syndrome Finding site Skeletal muscle structure false Inferred relationship Some 4
Mitochondrial myopathy, lactic acidosis, deafness syndrome Finding site Structure of auditory system (body structure) true Inferred relationship Some 2
Mitochondrial myopathy, lactic acidosis, deafness syndrome Finding site Skeletal muscle structure true Inferred relationship Some 3
Mitochondrial myopathy, lactic acidosis, deafness syndrome Interprets Hearing true Inferred relationship Some 1
Mitochondrial myopathy, lactic acidosis, deafness syndrome Has interpretation Impaired true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start