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66091009: Congenital disease (disorder)


Status: current. Date: 31-Jul 2002

Descriptions:

Id Description Lang Type Status Case? Module
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
109767019 Congenital disease, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500309015 Congenital abnormality en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
500310013 Fetal developmental abnormality en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011638011 Foetal developmental abnormality en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core


122 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disease Is a Fetal and/or neonatal disorder true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Congenital disease Occurrence Congenital true Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital infectious disease Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Joubert syndrome (disorder) Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Sickling disorder due to hemoglobin S (disorder) Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Congenital anomaly of liver Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Severe combined immunodeficiency with low T- and B-cell numbers Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Congenital omphalocele Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Congenital abnormality of ventricles and ventricular septum Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Congenital atrophy of left lobe of liver Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Multiple system malformation syndrome Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Inborn error of metabolism Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly
Orofacial cleft (disorder) Is a True Congenital disease Congenital syphilitic hepatomegaly Congenital syphilitic hepatomegaly

This concept is not in any reference sets

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