FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

42681006: Islet cell hyperplasia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
71210016 Islet cell hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
71212012 Nesidioblastosis en Synonym Active Entire term case insensitive SNOMED CT core module
493413019 Pancreatic endocrine cell hyperplasia en Synonym Active Entire term case insensitive SNOMED CT core module
779607010 Islet cell hyperplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Islet cell hyperplasia Is a Congenital anomaly of pancreas false Inferred relationship Existential restriction modifier
Islet cell hyperplasia Is a Disorder of endocrine pancreas true Inferred relationship Existential restriction modifier
Islet cell hyperplasia Occurrence Congenital false Inferred relationship Existential restriction modifier
Islet cell hyperplasia Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Islet cell hyperplasia Finding site Endocrine pancreatic structure false Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 2
Islet cell hyperplasia Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier
Islet cell hyperplasia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Is a Congenital anomaly of endocrine gland true Inferred relationship Existential restriction modifier
Islet cell hyperplasia Occurrence Congenital false Inferred relationship Existential restriction modifier
Islet cell hyperplasia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Islet cell hyperplasia Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 2
Islet cell hyperplasia Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Islet cell hyperplasia Is a Congenital malformation of pancreas true Inferred relationship Existential restriction modifier
Islet cell hyperplasia Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier 3
Islet cell hyperplasia Finding site Endocrine pancreatic structure false Inferred relationship Existential restriction modifier 3
Islet cell hyperplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Finding site Endocrine pancreatic structure false Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1
Islet cell hyperplasia Finding site Endocrine pancreas cell true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hyperplasia of islet alpha cells with gastrin excess Is a True Islet cell hyperplasia Inferred relationship Existential restriction modifier
Hyperplasia of pancreatic islet beta cell Is a True Islet cell hyperplasia Inferred relationship Existential restriction modifier
Hyperplasia of islet alpha cells with glucagon excess Is a True Islet cell hyperplasia Inferred relationship Existential restriction modifier
Hyperinsulinism due to focal adenomatous hyperplasia Is a True Islet cell hyperplasia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start