302961007: Hereditary splenic hypoplasia (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Digestive system finding (finding)\maladie de l'appareil digestif\...
• \Digestive system hereditary disorder\Hereditary splenic hypoplasia
• \Congenital anomaly of digestive system\Hereditary splenic hypoplasia
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary splenic hypoplasia
• \Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Hereditary splenic hypoplasia
• \Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary splenic hypoplasia
• \Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Hereditary splenic hypoplasia
• \Disease\affection d'un système corporel\maladie de l'appareil digestif\Congenital anomaly of digestive system\Hereditary splenic hypoplasia
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of digestive system\Hereditary splenic hypoplasia
• \Disease\trouble du développement\Developmental hereditary disorder\Hereditary splenic hypoplasia
• \Disease\trouble du développement\Congenital malformation\Congenital anomaly of digestive system\Hereditary splenic hypoplasia

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
445000018	Hereditary splenic hypoplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
699145015	Hereditary splenic hypoplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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