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763839005: Neonatal Marfan syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3644679014 Neonatal Marfan syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3644680012 Neonatal Marfan syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3644681011 A rare severe and life-threatening genetic disease occurring during the neonatal period. The disease has characteristics of classical Marfan syndrome manifestations in addition to facial dysmorphism (megalocornea, iridodonesis, ectopia lentis, crumpled ears, loose redundant skin giving a 'senile' facial appearance), flexion joint contractures, pulmonary emphysema and a severe, rapidly progressive cardiovascular disease (including ascending aortic dilatation and severe mitral and/or tricuspid valve insufficiency). Additionally, skeletal manifestations (arachnodactyly, dolichostenomelia, pectus deformities) are also associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4136071000052119 Marfans syndrom hos nyfödd sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal Marfan syndrome Is a Congenital anomaly of cardiovascular system true Inferred relationship Some
Neonatal Marfan syndrome Is a Marfan's syndrome true Inferred relationship Some
Neonatal Marfan syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Neonatal Marfan syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Neonatal Marfan syndrome Is a Congenital connective tissue disorder true Inferred relationship Some
Neonatal Marfan syndrome Is a Neonatal cardiovascular disorder true Inferred relationship Some
Neonatal Marfan syndrome Occurrence Neonatal true Inferred relationship Some 4
Neonatal Marfan syndrome Occurrence Congenital true Inferred relationship Some 1
Neonatal Marfan syndrome Occurrence Congenital true Inferred relationship Some 2
Neonatal Marfan syndrome Associated morphology utvecklingsabnormitet false Inferred relationship Some 2
Neonatal Marfan syndrome Finding site Face structure true Inferred relationship Some 2
Neonatal Marfan syndrome Associated morphology utvecklingsabnormitet false Inferred relationship Some 3
Neonatal Marfan syndrome Occurrence Congenital true Inferred relationship Some 3
Neonatal Marfan syndrome Finding site Connective tissue structure false Inferred relationship Some 1
Neonatal Marfan syndrome Finding site Structure of cardiovascular system (body structure) false Inferred relationship Some 2
Neonatal Marfan syndrome Finding site Connective tissue structure true Inferred relationship Some 3
Neonatal Marfan syndrome Finding site Structure of cardiovascular system (body structure) true Inferred relationship Some 1
Neonatal Marfan syndrome Finding site Face structure false Inferred relationship Some 3
Neonatal Marfan syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Neonatal Marfan syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Neonatal Marfan syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Neonatal Marfan syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Neonatal Marfan syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Neonatal Marfan syndrome Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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