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36976004: Hypoparathyroidism (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
61678012 Hypoparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
61680018 Deficiency of parathyroid hormone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
61681019 Deficiency of parathyrin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768789012 Hypoparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5245688017 Deficiency of PTH (parathyroid hormone) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
61678012 Hypoparathyroidism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
61678012 Hypoparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
61680018 Deficiency of parathyroid hormone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
61680018 Deficiency of parathyroid hormone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
61681019 Deficiency of parathyrin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
61681019 Deficiency of parathyrin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
61682014 Deficiency of PTH en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
768789012 Hypoparathyroidism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
768789012 Hypoparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5245688017 Deficiency of PTH (parathyroid hormone) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
423131000274115 Hypoparathyreoidismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
460131000274115 Nebenschilddrüseninsuffizienz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
468111000274114 Nebenschilddrüsenunterfunktion de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
373351000172112 hypoparathyroïdie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
373351000172112 hypoparathyroïdie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
423131000274115 Hypoparathyreoidismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
460131000274115 Nebenschilddrüseninsuffizienz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
468111000274114 Nebenschilddrüsenunterfunktion de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

37 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypoparathyroidism Is a Disorder of parathyroid gland (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism Interprets Nutritional deficiency state false Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism Finding site Parathyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypoparathyroidism Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism Interprets Hormone secretion true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism Is a Decreased hormone secretion true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Post-surgical hypoparathyroidism Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic hypoparathyroidism Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism - X-linked Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism - autosomal dominant Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Polyglandular autoimmune syndrome, type 1 Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Transient hypoparathyroidism Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Postablative hypoparathyroidism Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Parathyroid hypocalcemic tetany Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hypoparathyroidism Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Autoimmune hypoparathyroidism Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Isolated late onset hypoparathyroidism (disorder) Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic parathyroidism Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism NOS Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
[X]Other hypoparathyroidism Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Cataract in hypoparathyroidism Associated with True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism due to impaired PTH secretion Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Is a False Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism due to hemochromatosis (disorder) Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Secondary hypoparathyroidism (disorder) Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism due to granulomatous disease (disorder) Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993. Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism following procedure (disorder) Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
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. Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism, deafness, renal disease syndrome (disorder) Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Hypoparathyroidism due to Wilson disease Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Sanjad Sakati syndrome Is a True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept)
Chorea due to hypoparathyroidism (disorder) Due to True Hypoparathyroidism Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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