21634003: Borjeson-Forssman-Lehmann syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Mental state, behavior and/or psychosocial function finding\Behavior finding\Intellectual disability\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\Congenital anomaly of central nervous system\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome

\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disorder of head\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome

\Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Borjeson-Forssman-Lehmann syndrome
\Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\Borjeson-Forssman-Lehmann syndrome
\Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\Borjeson-Forssman-Lehmann syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\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\X-linked hereditary disease\X-linked recessive hereditary disease\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Disorder of head\Disorder of brain\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Borjeson-Forssman-Lehmann syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Congenital anomaly of brain\Borjeson-Forssman-Lehmann syndrome
\Disease\Developmental 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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

36300015 Borjeson-Forssman-Lehmann syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

750951014 Borjeson-Forssman-Lehmann syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

1222652011 Borjeson syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

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
Borjeson-Forssman-Lehmann syndrome	Is a	Congenital anomaly of nervous system	false	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Is a	Congenital anomaly of head	false	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Is a	Mental retardation	false	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Is a	Congenital anomaly of brain	true	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	2
Borjeson-Forssman-Lehmann syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Is a	Intellectual disability	true	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Borjeson-Forssman-Lehmann syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Existential restriction modifier
Borjeson-Forssman-Lehmann syndrome	Interprets	Intellectual ability	true	Inferred relationship	Existential restriction modifier	2
Borjeson-Forssman-Lehmann syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	2
Borjeson-Forssman-Lehmann syndrome	Interprets	Adaptation behavior	true	Inferred relationship	Existential restriction modifier	3
Borjeson-Forssman-Lehmann syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
36300015	Borjeson-Forssman-Lehmann syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
750951014	Borjeson-Forssman-Lehmann syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
1222652011	Borjeson syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module