15771004: Diabetes insipidus (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

26721014 Diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

477505014 DI - Diabetes insipidus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

742658019 Diabetes insipidus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2997771000005113 diabetes insipidus da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
diabetes insipidus	Is a	Disorder of posterior pituitary	false	Inferred relationship	Some
diabetes insipidus	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
diabetes insipidus	Finding site	Neurohypophysis structure	false	Inferred relationship	Some	1
diabetes insipidus	Interprets	Nutritional deficiency (finding)	false	Inferred relationship	Some
diabetes insipidus	Is a	Metabolic disorder of transport	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Secondary arginine vasopressin-related polyuria (disorder)	Is a	False	diabetes insipidus	Inferred relationship	Some
Familial vasopressin-related polyuria	Is a	False	diabetes insipidus	Inferred relationship	Some
Vasopressin deficiency	Is a	False	diabetes insipidus	Inferred relationship	Some
A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Two types of Wolfram syndrome may be distinguished: type 1 (WS1) and type 2 (WS2). Two causative genes have been identified: WFS1 (4p16.1) and CISD2 (4q24). The clinical criteria for Wolfram syndrome diagnosis are juvenile-onset diabetes mellitus and optic atrophy, family history of Wolfram syndrome or diabetes mellitus and deafness. Transmission is autosomal recessive.	Is a	False	diabetes insipidus	Inferred relationship	Some
Idiopathic arginine vasopressin-related polyuria (disorder)	Is a	False	diabetes insipidus	Inferred relationship	Some
Primary polydipsia	Is a	False	diabetes insipidus	Inferred relationship	Some
Hypohidrosis-diabetes insipidus syndrome	Is a	False	diabetes insipidus	Inferred relationship	Some
Arginine vasopressin resistance (disorder)	Is a	False	diabetes insipidus	Inferred relationship	Some
Partial vasopressin-related polyuria	Is a	False	diabetes insipidus	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)