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363080007: hereditaire aandoening van spijsverteringsstelsel (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Digestive system finding (finding)\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Digestive system hereditary disorder (disorder)	Is a	Hereditary disorder by system	true	Inferred relationship	Some
Digestive system hereditary disorder (disorder)	Is a	Disorder of digestive system (disorder)	true	Inferred relationship	Some
Digestive system hereditary disorder (disorder)	Finding site	Structure of digestive system (body structure)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glucagon receptor-related hyperglucagonemia (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
FTH1-related iron overload	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Alstrom syndrome	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Caroli syndrome	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Infantile multisystem neurologic, endocrine, pancreatic disease (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Familial gastric type 1 neuroendocrine neoplasm	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Hereditary well-differentiated neuroendocrine tumor of small intestine (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Digenic haemochromatosis	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Glucose-galactose malabsorption	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
familiair maagcarcinoom	Is a	False	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Familial malignant tumor of colon (disorder)	Is a	False	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Cystic fibrosis with liver disease (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Cystic fibrosis with constipation	Is a	False	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Cystic fibrosis with distal intestinal obstruction syndrome (disorder)	Is a	False	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Growth retardation, intellectual developmental disorder and hepatopathy syndrome (disorder)	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some
Cystic fibrosis with intestinal findings	Is a	True	Digestive system hereditary disorder (disorder)	Inferred relationship	Some

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Id	Description	Lang	Type	Status	Case?	Module
482215018	Digestive system hereditary disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
754864016	Digestive system hereditary disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6471351000146112	hereditaire aandoening van spijsverteringsstelsel (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6471361000146110	hereditaire aandoening van spijsverteringsstelsel	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6471371000146116	erfelijke ziekte van maag-darmkanaal	nl	Synonym (core metadata concept)	Inactive	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6471381000146119	erfelijke aandoening van tractus digestivus	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6471391000146117	erfelijke aandoening van systema digestorium	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)