1208934006: Sagliker syndrome (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

5013621018 Sagliker syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

5013622013 Sagliker syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5013623015 A rare bone disease characterized by secondary hyperparathyroidism in patients with chronic renal failure, caused by improper treatment in the early stages of the disease with retention of phosphorus, vitamin D deficiency and disturbed calcium-phosphorus metabolism, which result in increased parathyroid hormone levels. Patients present with short stature, severe changes of the skull and jaws as well as other skeletal deformities, dental anomalies, brown tumors in the mouth, hearing loss, and neuropsychiatric disorders. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5013624014 A rare bone disease characterised by secondary hyperparathyroidism in patients with chronic renal failure, caused by improper treatment in the early stages of the disease with retention of phosphorus, vitamin D deficiency and disturbed calcium-phosphorus metabolism, which result in increased parathyroid hormone levels. Patients present with short stature, severe changes of the skull and jaws as well as other skeletal deformities, dental anomalies, brown tumours in the mouth, hearing loss, and neuropsychiatric disorders. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5620831000052119 Sagliker-syndromet sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sagliker syndrome (disorder)	Finding site	Bone structure	true	Inferred relationship	Some	1
Sagliker syndrome (disorder)	Is a	Renal osteodystrophy	true	Inferred relationship	Some
Sagliker syndrome (disorder)	Is a	Hyperparathyroidism due to renal insufficiency	true	Inferred relationship	Some
Sagliker syndrome (disorder)	Clinical course	Chronic	true	Inferred relationship	Some	4
Sagliker syndrome (disorder)	Due to	Renal impairment	true	Inferred relationship	Some	7
Sagliker syndrome (disorder)	Finding site	Parathyroid structure	true	Inferred relationship	Some	5
Sagliker syndrome (disorder)	Finding site	Kidney structure	true	Inferred relationship	Some	6
Sagliker syndrome (disorder)	Interprets	Measurement of renal function	false	Inferred relationship	Some	2
Sagliker syndrome (disorder)	Has interpretation	Impaired	true	Inferred relationship	Some	2
Sagliker syndrome (disorder)	Interprets	Hormone secretion	true	Inferred relationship	Some	3
Sagliker syndrome (disorder)	Has interpretation	Increased	true	Inferred relationship	Some	3
Sagliker syndrome (disorder)	Associated morphology	Dystrophy	true	Inferred relationship	Some	1
Sagliker syndrome (disorder)	Interprets	Renal function	true	Inferred relationship	Some	2

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
5013621018	Sagliker syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5013622013	Sagliker syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5013623015	A rare bone disease characterized by secondary hyperparathyroidism in patients with chronic renal failure, caused by improper treatment in the early stages of the disease with retention of phosphorus, vitamin D deficiency and disturbed calcium-phosphorus metabolism, which result in increased parathyroid hormone levels. Patients present with short stature, severe changes of the skull and jaws as well as other skeletal deformities, dental anomalies, brown tumors in the mouth, hearing loss, and neuropsychiatric disorders.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5013624014	A rare bone disease characterised by secondary hyperparathyroidism in patients with chronic renal failure, caused by improper treatment in the early stages of the disease with retention of phosphorus, vitamin D deficiency and disturbed calcium-phosphorus metabolism, which result in increased parathyroid hormone levels. Patients present with short stature, severe changes of the skull and jaws as well as other skeletal deformities, dental anomalies, brown tumours in the mouth, hearing loss, and neuropsychiatric disorders.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5620831000052119	Sagliker-syndromet	sv	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)