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

840509001: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3902186018 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3902187010 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form 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
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Is a Disorder of adrenal cortex false Inferred relationship Existential restriction modifier
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Is a Congenital anomaly of adrenal gland true Inferred relationship Existential restriction modifier
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Existential restriction modifier 2
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form Is a Adrenocortical hyperplasia true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start