703254001: pseudohypoaldostéronisme type 2A (trouble)

SNOMED CT Concept\constatation clinique\Disease\trouble métabolique\trouble métabolique du transport\pseudohypoaldostéronisme\Pseudohypoaldosteronism, type 2\Pseudohypoaldosteronism type 2A

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3008116014 Pseudohypoaldosteronism type 2A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3008144010 Gordon hyperkalemia-hypertension syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3008151018 Pseudohypoaldosteronism type 2A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3008177014 Gordon hyperkalaemia-hypertension syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

733661000241111 pseudohypoaldostéronisme type 2A (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

943521000172118 PHA2A - pseudohypoaldostéronisme type 2A fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

945521000172119 pseudohypoaldostéronisme type 2A fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3008221015 An autosomal dominant disease characterized by increased serum potassium levels, hypertension, short stature, increased urinary calcium excretion and hyperchloremic metabolic acidosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3008224011 An autosomal dominant disease characterised by increased serum potassium levels, hypertension, short stature, increased urinary calcium excretion and hyperchloraemic metabolic acidosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pseudohypoaldosteronism type 2A	est un(e) (attribut)	Pseudohypoaldosteronism, type 2	true	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets