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715669000: Congenital epithelial dysplasia of intestine (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303361018 Congenital tufting enteropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303363015 Tufting enteropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303364014 Congenital epithelial dysplasia of intestine (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303365010 Congenital epithelial dysplasia of intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303366011 Intestinal epithelial dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303359010 A congenital enteropathy presenting with early-onset severe intractable diarrhea sometimes causing irreversible intestinal failure. Infants develop a watery diarrhea within the first days after birth and the diarrhea persists in spite of bowel rest and parenteral nutrition. Some infants are reported to have associated choanal, rectal or esophageal atresia. Autosomal recessive transmission but the causative gene has not been yet identified. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303360017 A congenital enteropathy presenting with early-onset severe intractable diarrhoea sometimes causing irreversible intestinal failure. Infants develop a watery diarrhoea within the first days after birth and the diarrhoea persists in spite of bowel rest and parenteral nutrition. Some infants are reported to have associated choanal, rectal or oesophageal atresia. Autosomal recessive transmission but the causative gene has not been yet identified. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
11360261000172117 dysplasie congénitale de l'épithélium intestinal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11360271000172114 dysplasie épithéliale congénitale de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11360281000172112 dysplasie épithéliale intestinale congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4631801000172115 congenitale intestinale epitheliale dysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital epithelial dysplasia of intestine (disorder) Is a Disorder of duodenum false Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Congenital disease (disorder) false Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Disorder of gastrointestinal tract mucous membrane (disorder) true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Soft tissue lesion true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Lesion of mucosa true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Disorder of soft tissue of trunk true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Disorder of jejunum (disorder) true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Associated morphology Epithelial dysplasia true Inferred relationship Some 2
Congenital epithelial dysplasia of intestine (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital epithelial dysplasia of intestine (disorder) Finding site Jejunal mucous membrane structure true Inferred relationship Some 2
Congenital epithelial dysplasia of intestine (disorder) Associated morphology Epithelial dysplasia false Inferred relationship Some 3
Congenital epithelial dysplasia of intestine (disorder) Occurrence Congenital false Inferred relationship Some 3
Congenital epithelial dysplasia of intestine (disorder) Finding site Duodenal mucous membrane structure false Inferred relationship Some 3
Congenital epithelial dysplasia of intestine (disorder) Is a Congenital anomaly of duodenum true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital epithelial dysplasia of intestine (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital epithelial dysplasia of intestine (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital epithelial dysplasia of intestine (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Congenital epithelial dysplasia of intestine (disorder) Finding site Duodenal mucous membrane structure true Inferred relationship Some 1
Congenital epithelial dysplasia of intestine (disorder) Associated morphology Epithelial dysplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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