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363627009: Parathyromatosis (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
484122017 Parathyromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
759820010 Parathyromatosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parathyromatosis Is a Ectopic hyperparathyroidism true Inferred relationship Existential restriction modifier
Parathyromatosis Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Parathyromatosis Finding site Parathyroid structure false Inferred relationship Existential restriction modifier 1
Parathyromatosis Finding site Ectopic endocrine structure false Inferred relationship Existential restriction modifier 1
Parathyromatosis Associated morphology Congenital ectopia (morphologic abnormality) false Inferred relationship Existential restriction modifier 1
Parathyromatosis Associated morphology Congenital ectopia (morphologic abnormality) false Inferred relationship Existential restriction modifier 2
Parathyromatosis Has definitional manifestation Increased hormone secretion false Inferred relationship Existential restriction modifier
Parathyromatosis Associated morphology Congenital ectopia (morphologic abnormality) false Inferred relationship Existential restriction modifier 2
Parathyromatosis Associated morphology Congenital ectopia (morphologic abnormality) false Inferred relationship Existential restriction modifier 2
Parathyromatosis Associated morphology Congenital ectopia (morphologic abnormality) false Inferred relationship Existential restriction modifier 2
Parathyromatosis Is a Congenital anomaly of parathyroid glands false Inferred relationship Existential restriction modifier
Parathyromatosis Occurrence Congenital false Inferred relationship Existential restriction modifier
Parathyromatosis Associated morphology Congenital ectopia false Inferred relationship Existential restriction modifier 1
Parathyromatosis Associated morphology Congenital ectopia false Inferred relationship Existential restriction modifier 1
Parathyromatosis Finding site Parathyroid structure false Inferred relationship Existential restriction modifier 1
Parathyromatosis Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Parathyromatosis Associated morphology Congenital ectopia true Inferred relationship Existential restriction modifier 2
Parathyromatosis Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Parathyromatosis Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
Parathyromatosis Has interpretation Increased true Inferred relationship Existential restriction modifier 1
Parathyromatosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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