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42183005: Pseudohypoparathyroidism type II (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
70396015 Pseudohypoparathyroidism type II en Synonym Active Only initial character case insensitive SNOMED CT core module
779054013 Pseudohypoparathyroidism type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3786606017 Pseudohypoparathyroidism type 2 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pseudohypoparathyroidism type II Is a Pseudohypoparathyroidism type I A false Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type II Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Occurrence Congenital false Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type II Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier
Pseudohypoparathyroidism type II Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Finding site Structure of endocrine system false Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type II Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type II Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Has interpretation Decreased true Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type II Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
Pseudohypoparathyroidism type II Is a Pseudohypoparathyroidism 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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