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1228876007: Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5063561014 Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5063562019 Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
5063564018 Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
5063565017 Interstitial lung and liver disease en Synonym Active Entire term case insensitive SNOMED CT core module
5063566016 Hereditary pulmonary alveolar proteinosis with hepatic involvement en Synonym Active Entire term case insensitive SNOMED CT core module
5063567013 Pulmonary alveolar proteinosis Reunion island type 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
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Is a Pulmonary alveolar proteinosis true Inferred relationship Existential restriction modifier
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Is a Interstitial lung disease true Inferred relationship Existential restriction modifier
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Is a Hereditary disorder by system true Inferred relationship Existential restriction modifier
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Is a Chronic lung disease true Inferred relationship Existential restriction modifier
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Finding site Structure of interstitial tissue of lung true Inferred relationship Existential restriction modifier 3
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Finding site Pulmonary alveolar structure true Inferred relationship Existential restriction modifier 1
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Associated morphology Protein deposition 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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