21634003: Borjeson-Forssman-Lehmann syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome

\Mental state, behavior and/or psychosocial function finding (finding)\Behavior finding\Intelligenzminderung\Borjeson-Forssman-Lehmann syndrome

\Central nervous system finding\Finding of brain\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome

\Functional finding\Cognitive function finding (finding)\Impaired cognition (finding)\Intelligenzminderung\Borjeson-Forssman-Lehmann syndrome
\Functional finding\Cognitive function finding (finding)\Intellectual ability - finding\Intelligenzminderung\Borjeson-Forssman-Lehmann syndrome
\Functional finding\Intelligence finding\Intellectual ability - finding\Intelligenzminderung\Borjeson-Forssman-Lehmann syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Borjeson-Forssman-Lehmann syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Borjeson-Forssman-Lehmann syndrome
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder (disorder)\X-linked hereditary disease\X-linked recessive hereditary disease\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Congenital anomaly of nervous system\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of head (disorder)\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder (disorder)\Neurodevelopmental disorder\Intelligenzminderung\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Borjeson-Forssman-Lehmann syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Is a	Congenital anomaly of nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Is a	Congenital anomaly of head	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Is a	retard mental	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Is a	Congenital anomaly of brain	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Borjeson-Forssman-Lehmann syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Borjeson-Forssman-Lehmann syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Is a	Intelligenzminderung	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Borjeson-Forssman-Lehmann syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Borjeson-Forssman-Lehmann syndrome	Interprets	Intellectual ability (observable entity)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Borjeson-Forssman-Lehmann syndrome	Has interpretation	Impaired (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Borjeson-Forssman-Lehmann syndrome	Interprets	Adaptation behavior	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Borjeson-Forssman-Lehmann syndrome	Has interpretation	Impaired (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
36300015	Borjeson-Forssman-Lehmann syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
750951014	Borjeson-Forssman-Lehmann syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1222652011	Borjeson syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
36300015	Borjeson-Forssman-Lehmann syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
196134011	BFLS	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
750951014	Borjeson-Forssman-Lehmann syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
750951014	Borjeson-Forssman-Lehmann syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1222652011	Borjeson syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1222652011	Borjeson syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3409551001000114	Borjeson-Forssman-Lehmann-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
926671000172112	BFLS - Borjeson-Forssman-Lehmann syndrome	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
939241000172110	syndrome de Borjeson-Forssman-Lehmann	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
926671000172112	BFLS - Borjeson-Forssman-Lehmann syndrome	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
939241000172110	syndrome de Borjeson-Forssman-Lehmann	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3409551001000114	Borjeson-Forssman-Lehmann-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module