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25744000: Hereditary gastrogenic lactose intolerance (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
43143014 Hereditary gastrogenic lactose intolerance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
43144015 Severe familial lactose intolerance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
756097018 Hereditary gastrogenic lactose intolerance (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3754810012 A very rare disorder which is probably hereditary. It is not caused by a disorder of disaccharidease activity or by impairment of monosaccharide transport but rather by abnormal permeability of lactose through the gastric mucosa. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
43143014 Hereditary gastrogenic lactose intolerance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
43143014 Hereditary gastrogenic lactose intolerance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
43144015 Severe familial lactose intolerance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
43144015 Severe familial lactose intolerance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
756097018 Hereditary gastrogenic lactose intolerance (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
756097018 Hereditary gastrogenic lactose intolerance (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3754810012 A very rare disorder which is probably hereditary. It is not caused by a disorder of disaccharidease activity or by impairment of monosaccharide transport but rather by abnormal permeability of lactose through the gastric mucosa. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
6259991000241119 intolérance héréditaire au lactose d'origine gastrogénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6259991000241119 intolérance héréditaire au lactose d'origine gastrogénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary gastrogenic lactose intolerance (disorder) Is a intolérance au lactose false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Disorder of carbohydrate transport false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Severity Severe false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Stomach finding false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Finding site Gastric mucous membrane structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary gastrogenic lactose intolerance (disorder) Is a Intolerance to lactose in children without lactase deficiency (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Mucosal finding false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a General finding of soft tissue false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Associated with Lactose true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary gastrogenic lactose intolerance (disorder) Is a Disorder of stomach (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Disorder of soft tissue of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Disorder of gastrointestinal tract mucous membrane (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary gastrogenic lactose intolerance (disorder) Is a Disorder of soft tissue of abdominal cavity (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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