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Terminology chevron_right Concepts chevron_right 367417005

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Component

367417005

The component that hold information about this concept.

Fully Specified Name (FSN)

Propionyl-coa carboxylase deficiency (disorder)

Shortest Term

Propionic acidemia, type i

Definition Status

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

Summary

Propionyl-coa carboxylase deficiency (disorder)

SCTID: 367417005, Primitive, Inactive

367417005|Propionyl-coa carboxylase deficiency (disorder)|

en Propionyl-coa carboxylase deficiency
en Propionyl-coa carboxylase deficiency (disorder)
en Hyperglycinaemia with ketosis and leucopenia, types i and ii
en Hyperglycinemia with ketosis and leukopenia, types i and ii
en Ketotic glycinaemia, types i and ii
en Ketotic glycinemia, types i and ii
en Propionic acidaemia, type i
en Propionic acidaemia, type ii
en Propionic acidemia, type i
en Propionic acidemia, type ii

Expression

367417005 |Propionyl-coa carboxylase deficiency (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2769729011 - Propionyl-CoA carboxylase deficiency (en) View
2769729011	en	Synonym (core metadata concept)	Propionyl-CoA carboxylase deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2741499010 - Propionyl-CoA carboxylase deficiency (disorder) (en) View
2741499010	en	Fully specified name (core metadata concept)	Propionyl-CoA carboxylase deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2671104014 - Propionyl-CoA carboxylase deficiency [dup] (en) View
2671104014	en	Synonym (core metadata concept)	Propionyl-CoA carboxylase deficiency [dup]	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
775490017 - Propionyl-CoA carboxylase deficiency [dup] (disorder) (en) View
775490017	en	Fully specified name (core metadata concept)	Propionyl-CoA carboxylase deficiency [dup] (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
491935014 - Propionyl-CoA carboxylase deficiency (disorder) (en) View
491935014	en	Synonym (core metadata concept)	Propionyl-CoA carboxylase deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
491929014 - Hyperglycinaemia with ketosis and leucopenia, types I and II (en) View
491929014	en	Synonym (core metadata concept)	Hyperglycinaemia with ketosis and leucopenia, types I and II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491932012 - Hyperglycinemia with ketosis and leukopenia, types I and II (en) View
491932012	en	Synonym (core metadata concept)	Hyperglycinemia with ketosis and leukopenia, types I and II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491930016 - Ketotic glycinaemia, types I and II (en) View
491930016	en	Synonym (core metadata concept)	Ketotic glycinaemia, types I and II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491933019 - Ketotic glycinemia, types I and II (en) View
491933019	en	Synonym (core metadata concept)	Ketotic glycinemia, types I and II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491927011 - Propionic acidaemia, type I (en) View
491927011	en	Synonym (core metadata concept)	Propionic acidaemia, type I	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491928018 - Propionic acidaemia, type II (en) View
491928018	en	Synonym (core metadata concept)	Propionic acidaemia, type II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491931017 - Propionic acidemia, type I (en) View
491931017	en	Synonym (core metadata concept)	Propionic acidemia, type I	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
491934013 - Propionic acidemia, type II (en) View
491934013	en	Synonym (core metadata concept)	Propionic acidemia, type II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (211600029) - 367417005 -> 363136009 (116680003) View
116680003 \|Is a (attribute)\|	363136009 \|Hereditary disorder of hematologic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211601025) - 367417005 -> 84828003 (116680003) View
116680003 \|Is a (attribute)\|	84828003 \|Leukopenia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211602021) - 367417005 -> 64654004 (116680003) View
116680003 \|Is a (attribute)\|	64654004 \|Hyperglycinemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211603027) - 367417005 -> 69080001 (116680003) View
116680003 \|Is a (attribute)\|	69080001 \|Propionic acidemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211604022) - 367417005 -> 40888008 (116680003) View
116680003 \|Is a (attribute)\|	40888008 \|Congenital anomaly of the hematopoietic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211605023) - 367417005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211606024) - 367417005 -> 78548001 (116680003) View
116680003 \|Is a (attribute)\|	78548001 \|Enzymopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (769545029) - 367417005 -> 52501007 (363698007) View
363698007 \|Finding site (attribute)\|	52501007 \|Leukocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (769546028) - 367417005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (769547021) - 367417005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (211600029) - 367417005 -> 363136009 (116680003) View
116680003 \|Is a (attribute)\|	363136009 \|Hereditary disorder of hematologic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211601025) - 367417005 -> 84828003 (116680003) View
116680003 \|Is a (attribute)\|	84828003 \|Leukopenia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211602021) - 367417005 -> 64654004 (116680003) View
116680003 \|Is a (attribute)\|	64654004 \|Hyperglycinemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211603027) - 367417005 -> 69080001 (116680003) View
116680003 \|Is a (attribute)\|	69080001 \|Propionic acidemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211604022) - 367417005 -> 40888008 (116680003) View
116680003 \|Is a (attribute)\|	40888008 \|Congenital anomaly of the hematopoietic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211605023) - 367417005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211606024) - 367417005 -> 78548001 (116680003) View
116680003 \|Is a (attribute)\|	78548001 \|Enzymopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (769545029) - 367417005 -> 52501007 (363698007) View
363698007 \|Finding site (attribute)\|	52501007 \|Leukocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (769546028) - 367417005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (769547021) - 367417005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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