717792007: Pseudohypoparathyroidism type 1C (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of neck region\Disease of neck\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type 1C (disorder)

\Functional finding\Decline in functional status (finding)\Decreased hormone secretion\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type 1C (disorder)

\Endocrine finding\Decreased hormone secretion\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type 1C (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pseudohypoparathyroidism type 1C (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Pseudohypoparathyroidism type 1C (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pseudohypoparathyroidism type 1C (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Hereditary disorder of endocrine system (disorder)\Pseudohypoparathyroidism type 1C (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type 1C (disorder)
\Disease\Disease of neck\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type 1C (disorder)
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Disorder of calcium metabolism (disorder)\Hypocalcemia\Pseudohypoparathyroidism\Pseudohypoparathyroidism type 1C (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

3310264019 Pseudohypoparathyroidism type 1C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3310265018 Pseudohypoparathyroidism type 1C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3310264019 Pseudohypoparathyroidism type 1C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3310265018 Pseudohypoparathyroidism type 1C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3422841001000111 Pseudohypoparathyreoidismus Typ 1C de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

945281000172118 pseudohypoparathyroïdie type 1C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

945281000172118 pseudohypoparathyroïdie type 1C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3422841001000111 Pseudohypoparathyreoidismus Typ 1C de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pseudohypoparathyroidism type 1C (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type 1C (disorder)	Is a	Pseudohypoparathyroidism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type 1C (disorder)	Finding site	Parathyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type 1C (disorder)	Interprets	Hormone secretion	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type 1C (disorder)	Has interpretation	Decreased	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type 1C (disorder)	Is a	Hereditary disorder by system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type 1C (disorder)	Is a	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

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This concept is not in any reference sets