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363080007: Digestive system hereditary disorder (disorder)


Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
482215018 Digestive system hereditary disorder en Synonym Active Case insensitive SNOMED CT core
754864016 Digestive system hereditary disorder (disorder) en Fully specified name Active Case insensitive SNOMED CT core


348 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital deafness with labyrinthine aplasia, microtia and microdontia Is a False Digestive system hereditary disorder Inferred relationship Some
Choanal atresia with radial ray hypoplasia Is a True Digestive system hereditary disorder Inferred relationship Some
Familial omphalocele syndrome with facial dysmorphism Is a True Digestive system hereditary disorder Inferred relationship Some
Dentin dysplasia with sclerotic bone syndrome Is a False Digestive system hereditary disorder Inferred relationship Some
Poikiloderma, alopecia, retrognathism, cleft palate syndrome Is a False Digestive system hereditary disorder Inferred relationship Some
Pilodental dysplasia, refractive errors syndrome Is a False Digestive system hereditary disorder Inferred relationship Some
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome Is a True Digestive system hereditary disorder Inferred relationship Some
Ectodermal dysplasia syndactyly syndrome Is a False Digestive system hereditary disorder Inferred relationship Some

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Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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