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 |
| 446451000241114 | pseudohypoparathyroïdie (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 493731000172119 | pseudohypoparathyroïdie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 498307013 | Constitutional chronic hypocalcaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 797767018 | Pseudohypoparathyroidism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 98005010 | Pseudohypoparathyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 98008012 | Constitutional chronic hypocalcemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 98009016 | Familial pseudohypoparathyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 98010014 | Parathyroid hormone resistant hypoparathyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3786612010 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3786613017 | A heterogeneous group of endocrine disorders with characteristics of normal renal function and resistance to the action of parathyroid hormone (PTH), manifesting with hypocalcemia, hyperphosphatemia 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| pseudohypoparathyroïdie (trouble) | interprète (attribut) | Hormone secretion | true | Inferred relationship | Some | 1 | |
| pseudohypoparathyroïdie (trouble) | localisation d'une constatation (attribut) | Parathyroid structure | true | Inferred relationship | Some | 2 | |
| pseudohypoparathyroïdie (trouble) | a pour interprétation (attribut) | Decreased | true | Inferred relationship | Some | 1 | |
| pseudohypoparathyroïdie (trouble) | est un(e) (attribut) | hypoparathyroïdie | true | Inferred relationship | Some | ||
| pseudohypoparathyroïdie (trouble) | est un(e) (attribut) | hypocalcémie (trouble) | true | Inferred relationship | Some | ||
| pseudohypoparathyroïdie (trouble) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Pseudohypoparathyroidism type II | est un(e) (attribut) | True | pseudohypoparathyroïdie (trouble) | Inferred relationship | Some | |
| pseudohypoparathyroïdie type 1B (trouble) | est un(e) (attribut) | True | pseudohypoparathyroïdie (trouble) | Inferred relationship | Some | |
| pseudohypoparathyroïdie type 1A (trouble) | est un(e) (attribut) | True | pseudohypoparathyroïdie (trouble) | Inferred relationship | Some | |
| Pseudopseudohypoparathyroidism | est un(e) (attribut) | True | pseudohypoparathyroïdie (trouble) | Inferred relationship | Some | |
| Pseudohypoparathyroidism type 1C (disorder) | est un(e) (attribut) | True | pseudohypoparathyroïdie (trouble) | Inferred relationship | Some | |
| Cataract due to pseudohypoparathyroidism (disorder) | Due to | True | pseudohypoparathyroïdie (trouble) | Inferred relationship | Some | 2 |
Reference Sets
FHIR