68985000: Benign neonatal hyperaminoaciduria (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

114590018 Benign neonatal hyperaminoaciduria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

808880014 Benign neonatal hyperaminoaciduria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

114590018 Benign neonatal hyperaminoaciduria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

114590018 Benign neonatal hyperaminoaciduria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

808880014 Benign neonatal hyperaminoaciduria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

808880014 Benign neonatal hyperaminoaciduria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign neonatal hyperaminoaciduria	Is a	troubles endocriniens et/ou métaboliques spécifiques au fœtus ou au nouveau-né	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Hereditary disorder of endocrine system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Reproductive system hereditary disorder (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Amino acid transport disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Inborn error of amino acid metabolism	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Occurrence	Neonatal	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Benign neonatal hyperaminoaciduria	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Neonatal disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Aminoaciduria	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Occurrence	Neonatal	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Benign neonatal hyperaminoaciduria	Is a	Inherited aminoaciduria (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign neonatal hyperaminoaciduria	Is a	Neonatal metabolic disorder (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set