718848000: Fried syndrome (disorder)

\Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome

\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disorder of head\Disorder of brain\Hydrocephalus\Fried syndrome

\Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Fried syndrome
\Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\Fried syndrome
\Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\Fried syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Fried syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Fried syndrome
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Fried syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Fried syndrome
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Fried syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Hydrocephalus\Fried syndrome
\Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disease\Disorder of head\Disorder of brain\Hydrocephalus\Fried syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Fried syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Fried syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Fried syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Fried syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3314123013 Fried syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3314124019 Fried syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Fried syndrome	Is a	Mental retardation	false	Inferred relationship	Existential restriction modifier
Fried syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Existential restriction modifier
Fried syndrome	Is a	Intellectual disability	true	Inferred relationship	Existential restriction modifier
Fried syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	1
Fried syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Fried syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Existential restriction modifier
Fried syndrome	Is a	Hydrocephalus	true	Inferred relationship	Existential restriction modifier
Fried syndrome	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Fried syndrome	Is a	Multiple malformation syndrome with facial defects as major feature	true	Inferred relationship	Existential restriction modifier
Fried syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Fried syndrome	Finding site	Face structure	true	Inferred relationship	Existential restriction modifier	2
Fried syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2
Fried syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Fried syndrome	Finding site	Structure of brain cerebrospinal fluid pathway	true	Inferred relationship	Existential restriction modifier	1
Fried syndrome	Associated morphology	Dilatation	true	Inferred relationship	Existential restriction modifier	1
Fried syndrome	Interprets	Intellectual ability	true	Inferred relationship	Existential restriction modifier	3
Fried syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	3
Fried syndrome	Interprets	Adaptation behavior	true	Inferred relationship	Existential restriction modifier	4
Fried syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	4

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
3314123013	Fried syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3314124019	Fried syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module