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721155007: Congenital short esophagus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3324472011 Congenital short esophagus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324473018 Congenital short esophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324474012 Congenital short oesophagus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5915981000241111 œsophage court congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital short esophagus (disorder) Is a Congenital anomaly of esophagus true Inferred relationship Some
Congenital short esophagus (disorder) Is a Deformity (finding) false Inferred relationship Some
Congenital short esophagus (disorder) Associated morphology Abnormally short growth (morphologic abnormality) true Inferred relationship Some 1
Congenital short esophagus (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital short esophagus (disorder) Finding site Oesophageal structure true Inferred relationship Some 1
Congenital short esophagus (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital short esophagus (disorder) Is a Congenital deformity true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare syndromic esophageal malformation characterized by severe congenital brachyesophagus with midline diaphragmatic hernia and secondary intrathoracic stomach, and vertebral anomalies (in particular rachischisis of the cervical/thoracic spine). Additional reported manifestations include intrauterine growth restriction, short neck, intestinal malrotation, herniation of other abdominal organs, and cleft lip, among others. The condition is mostly fatal in the neonatal or early infantile period. Is a True Congenital short esophagus (disorder) Inferred relationship Some

This concept is not in any reference sets

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