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721234004: Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (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
3324723015 Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324724014 Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3324725010 Hyperinsulinism due to HNF1A deficiency 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
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Is a Hyperinsulinism true Inferred relationship Existential restriction modifier
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Finding site Endocrine pancreatic structure false Inferred relationship Existential restriction modifier
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Finding site Endocrine pancreatic structure true Inferred relationship Existential restriction modifier 1
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency Is a Congenital disease 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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