Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
415859016 | Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
672048012 | Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Is a | Acromesomelic dysplasia syndrome | false | Inferred relationship | Some | ||
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Is a | Pseudohypoparathyroidism and pseudopseudohypoparathyroidism | false | Inferred relationship | Some | ||
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Finding site | Bone structure | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Associated morphology | Dysplasia | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Finding site | Structure of endocrine system (body structure) | false | Inferred relationship | Some | 2 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Occurrence | Congenital | false | Inferred relationship | Some | ||
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Finding site | Skeletal system structure | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Finding site | Musculoskeletal structure of limb | false | Inferred relationship | Some | ||
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Is a | Congenital anomaly of endocrine gland | false | Inferred relationship | Some | ||
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Is a | Metabolic bone disease | false | Inferred relationship | Some | ||
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Finding site | Bone structure | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)