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Terminology chevron_right Concepts chevron_right 724172004

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724172004
The component that hold information about this concept.
Mcleod neuroacanthocytosis syndrome (disorder)
X-linked mcleod syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Mcleod neuroacanthocytosis syndrome (disorder)

SCTID: 724172004, Primitive, Active


724172004|Mcleod neuroacanthocytosis syndrome (disorder)|
  • en Mcleod neuroacanthocytosis syndrome
  • en Mcleod neuroacanthocytosis syndrome (disorder)
  • en X-linked mcleod syndrome

724172004 |Mcleod neuroacanthocytosis syndrome (disorder)|

<<< 1162976004 |X-linked recessive hereditary disease (disorder)| +
    11376001 |Hereditary acanthocytosis (disorder)| +
    70835005 |Disorder of basal ganglia (disorder)| +
    76349003 |Extrapyramidal disease (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 63599005 |Acanthocyte (cell)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

3431494011 - McLeod neuroacanthocytosis syndrome (en) View

3431494011
en
Synonym (core metadata concept)
McLeod neuroacanthocytosis syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3431493017 - McLeod neuroacanthocytosis syndrome (disorder) (en) View

3431493017
en
Fully specified name (core metadata concept)
McLeod neuroacanthocytosis syndrome (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3431495012 - X-linked McLeod syndrome (en) View

3431495012
en
Synonym (core metadata concept)
X-linked McLeod syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (13882884020) - 724172004 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (16350732022) - 724172004 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874388024) - 724172004 -> 128430005 (116680003) View

116680003 |Is a (attribute)|
128430005 |X-linked hereditary disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (14013765026) - 724172004 -> 1162976004 (116680003) View

116680003 |Is a (attribute)|
1162976004 |X-linked recessive hereditary disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874384021) - 724172004 -> 63599005 (116676008) View

116676008 |Associated morphology (attribute)|
63599005 |Acanthocyte (cell)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874390020) - 724172004 -> 32610002 (363698007) View

363698007 |Finding site (attribute)|
32610002 |Basal ganglion structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874391024) - 724172004 -> 41898006 (363698007) View

363698007 |Finding site (attribute)|
41898006 |Erythrocyte (cell)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874385022) - 724172004 -> 11376001 (116680003) View

116680003 |Is a (attribute)|
11376001 |Hereditary acanthocytosis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874386023) - 724172004 -> 70835005 (116680003) View

116680003 |Is a (attribute)|
70835005 |Disorder of basal ganglia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874387025) - 724172004 -> 76349003 (116680003) View

116680003 |Is a (attribute)|
76349003 |Extrapyramidal disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6874389027) - 724172004 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

1162976004 View

1162976004
X-linked recessive hereditary disease (disorder)
X-linked recessive hereditary disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

11376001 View

11376001
Hereditary acanthocytosis (disorder)
Hereditary acanthocytosis
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

70835005 View

70835005
Disorder of basal ganglia (disorder)
Disease of basal ganglia
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

76349003 View

76349003
Extrapyramidal disease (disorder)
Bệnh ngoại tháp
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

363235000 View

363235000
Hereditary disorder of nervous system (disorder)
Hereditary disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True
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