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717894000: Cataract due to pseudohypoparathyroidism (disorder)


Status: current, 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
3310533017 Cataract due to pseudohypoparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310534011 Cataract due to pseudohypoparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5816321000241110 cataracte due à une pseudohypoparathyroïdie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
524561000274111 Katarakt verursacht durch Martin-Albright-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601251000274110 Katarakt verursacht durch Pseudohypoparathyreoidismus de 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
Cataract due to pseudohypoparathyroidism (disorder) Due to A heterogeneous group of endocrine disorders with characteristics of normal renal function and resistance to the action of parathyroid hormone (PTH), manifesting with hypocalcaemia, hyperphosphataemia and elevated PTH levels and that includes the subtypes PHP type 1a (PHP-1a) , PHP type 1b (PHP-1b), PHP type 1c (PHP-1c), PHP type 2 (PHP-2) and pseudopseudohypoparathyroidism (PPHP). PHP-1a, PPHP, and PHP-1b are all due to molecular defects in the same locus of the GNAS (20q13.2-q13.3) gene coding the alpha sub-unit of the stimulatory G protein. PHP can be sporadic or inherited autosomal dominantly with parental imprinting. true Inferred relationship Some 2
Cataract due to pseudohypoparathyroidism (disorder) Is a Cataract true Inferred relationship Some
Cataract due to pseudohypoparathyroidism (disorder) Associated morphology Cataract false Inferred relationship Some 2
Cataract due to pseudohypoparathyroidism (disorder) Finding site Lens clear false Inferred relationship Some 2
Cataract due to pseudohypoparathyroidism (disorder) Finding site Lens clear true Inferred relationship Some 1
Cataract due to pseudohypoparathyroidism (disorder) Associated morphology Abnormally opaque structure (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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