57497006: Congenital anomaly of spleen (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Disorder of spleen\Congenital anomaly of spleen

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of spleen\Congenital anomaly of spleen
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Disorder of spleen\Congenital anomaly of spleen
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of spleen\Congenital anomaly of spleen
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of spleen\Congenital anomaly of spleen
\Finding of trunk structure\Disorder of trunk\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen

\Disease\Disorder of body system\Disorder of immune structure\Disorder of lymphoid system\Disorder of spleen\Congenital anomaly of spleen
\Disease\Disorder of body system\Disorder of hematopoietic structure\Disorder of lymphoid system\Disorder of spleen\Congenital anomaly of spleen
\Disease\Disorder of body system\Disorder of hematopoietic structure\Congenital anomaly of the hematopoietic system\Congenital anomaly of spleen
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of spleen\Congenital anomaly of spleen
\Disease\Disorder of trunk\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Congenital disease\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of the hematopoietic system\Congenital anomaly of spleen
\Disease\Developmental disorder\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of spleen
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of the hematopoietic system\Congenital anomaly of spleen

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

95610012 Congenital anomaly of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
95611011 Congenital anomaly of spleen, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
497905011 Congenital malformation of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
497906012 Anomalies of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
497907015 Congenital abnormality of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
796125013 Congenital anomaly of spleen (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital anomaly of spleen	Is a	Congenital anomaly of the hematopoietic system	true	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Is a	Disorder of spleen	true	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Finding site	Splenic structure	true	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Finding site	Structure of digestive system	false	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Is a	Congenital anomaly of abdomen	true	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Is a	Congenital anomaly of body cavity	false	Inferred relationship	Existential restriction modifier
Congenital anomaly of spleen	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Finding site	Splenic structure	false	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of spleen	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of spleen	Finding site	Splenic structure	false	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of spleen	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of spleen	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Accessory spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital splenomegaly	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital lobulation of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Splenogonadal fusion	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Ectopic spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital abnormal shape of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital absence of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital cyst of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital hypoplasia of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Congenital malposition of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Aberrant spleen	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Hypoplasia of spleen	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Mis-shapen spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Other specified anomalies of spleen	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Anomalies of spleen NOS	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Bilateral right-sidedness sequence	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Ectopic splenic tissue	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Aberrant spleen	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Aplasia of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Biliary atresia with splenic malformation syndrome	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Epidermoid cyst of spleen	Is a	True	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Anomalies of spleen NOS	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier
Other specified anomalies of spleen	Is a	False	Congenital anomaly of spleen	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
95610012	Congenital anomaly of spleen	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
95611011	Congenital anomaly of spleen, NOS	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
497905011	Congenital malformation of spleen	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
497906012	Anomalies of spleen	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
497907015	Congenital abnormality of spleen	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
796125013	Congenital anomaly of spleen (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module