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Terminology chevron_right Concepts chevron_right 1187567002

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1187567002
The component that hold information about this concept.
Autosomal recessive intermediate charcot-marie-tooth disease type d (disorder)
Autosomal recessive intermediate charcot-marie-tooth disease type d
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

Autosomal recessive intermediate charcot-marie-tooth disease type d (disorder)

SCTID: 1187567002, Primitive, Active


1187567002|Autosomal recessive intermediate charcot-marie-tooth disease type d (disorder)|
  • en Autosomal recessive intermediate charcot-marie-tooth disease type d
  • en Autosomal recessive intermediate charcot-marie-tooth disease type d (disorder)

1187567002 |Autosomal recessive intermediate charcot-marie-tooth disease type d (disorder)|

<<< 398100001 |Hereditary motor and sensory neuropathy (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 3058005 |Peripheral nervous system structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255398004 |Childhood (qualifier value)| }
Active

4674186016 - Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (en) View

4674186016
en
Synonym (core metadata concept)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

4674185017 - Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder) (en) View

4674185017
en
Fully specified name (core metadata concept)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

398100001 View

398100001
Hereditary motor and sensory neuropathy (disorder)
Hmsn
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (6b8dde20-958e-5226-800b-17e266da56f8) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G60.0
TRUE
ALWAYS G60.0
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
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