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717792007: Pseudohypoparathyroidism type 1C (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3310264019 Pseudohypoparathyroidism type 1C (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3310265018 Pseudohypoparathyroidism type 1C en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pseudohypoparathyroidism type 1C Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type 1C Is a Pseudohypoparathyroidism true Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type 1C Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type 1C Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type 1C Has interpretation Decreased true Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type 1C Is a Hereditary disorder by system false Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type 1C Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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