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717898002: Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (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
3310543019 Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310544013 Hereditary isolated hypoparathyroidism due to impaired parathormone secretion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5407680012 Familial isolated hypoparathyroidism due to impaired PTH (parathormone) secretion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310543019 Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310543019 Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310544013 Hereditary isolated hypoparathyroidism due to impaired parathormone secretion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310544013 Hereditary isolated hypoparathyroidism due to impaired parathormone secretion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5407680012 Familial isolated hypoparathyroidism due to impaired PTH (parathormone) secretion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6246131000241114 hypoparathyroïdie héréditaire isolée due à une altération de la sécrétion de l'hormone parathyroïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246141000241116 hypoparathyroïdie héréditaire isolée due à une altération de la sécrétion de parathormone fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246151000241118 hypoparathyroïdie héréditaire isolée due à une altération de la sécrétion de PTH (parathyroid hormone) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246131000241114 hypoparathyroïdie héréditaire isolée due à une altération de la sécrétion de l'hormone parathyroïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246141000241116 hypoparathyroïdie héréditaire isolée due à une altération de la sécrétion de parathormone fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246151000241118 hypoparathyroïdie héréditaire isolée due à une altération de la sécrétion de PTH (parathyroid hormone) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Is a Autosomal hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Is a Hypoparathyroidism false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Is a Hereditary disorder of endocrine system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Finding site Parathyroid structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Is a A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Interprets Evaluation procedure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Interprets Hormone secretion true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Finding site Parathyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Interprets Endocrine observable false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Is a Hypoparathyroidism due to impaired PTH secretion true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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