OMOP Concept 4031941
Disorder of glycoprotein metabolism
StandardConditionSNOMED238045003Disorder
Maps from
27
Descendants
88
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
27 source codes normalize to Disorder of glycoprotein metabolism via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Disorder of glycoprotein metabolism across source vocabularies.
- Disorder of glycoprotein metabolism (disorder)
- Glycoprotein metabolism disorder
- trastorno del metabolismo de las glicoproteínas
- trastorno del metabolismo de las glucoproteínas
- trastorno del metabolismo de las glucoproteínas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(9)Roll up to these when you need a wider cohort.
Narrower concepts
(88)Included automatically when you query with descendants.
- 1Alpha-1-antitrypsin deficiency
- 1Alpha-2-antitrypsin deficiency
- 1Autism spectrum disorder, epilepsy, arthrogryposis syndrome
- 1Carbohydrate-deficient glycoprotein syndrome
- 1Glycoprotein storage disorder
- 1Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- 1I-cell disease
- 1Larsen-like syndrome B3GAT3 type
- 1NGLY1-congenital disorder of deglycosylation
- 1Oligosaccharidosis
- 1Temtamy preaxial brachydactyly syndrome
- 2Alpha-N-acetylgalactosaminidase deficiency
- 2Aspartylglucosaminuria
- 2Beta-D-mannosidosis
- 2Carbohydrate-deficient glycoprotein syndrome type I
- 2Carbohydrate-deficient glycoprotein syndrome type II
- 2Carbohydrate-deficient glycoprotein syndrome type III
- 2Combined deficiency of sialidase AND beta galactosidase
- 2Early-onset epilepsy, intellectual disability, brain anomalies syndrome
- 2Fucosidosis
- 2Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome
- 2Jarcho-Levin syndrome
- 2Limb girdle muscular dystrophy due to POMK deficiency
- 2Mannosidosis
- 2Multiple congenital anomalies, hypotonia, seizures syndrome
- 2Multiple congenital anomalies, hypotonia, seizures syndrome type 2
- 2PGM3-related congenital disorder of glycosylation
- 2POGLUT1-related limb girdle muscular dystrophy R21
- 2Pseudo-Hurler polydystrophy
- 2Seizures, scoliosis, macrocephaly syndrome
- 2Sialidosis
- 2SLC35A1 congenital disorder of glycosylation
- 2XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation
- 3Adult fucosidosis
- 3ALG12-congenital disorder of glycosylation
- 3ALG1 congenital disorder of glycosylation
- 3ALG3 congenital disorder of glycosylation
- 3ALG8 congenital disorder of glycosylation
- 3ALG9 congenital disorder of glycosylation
- 3Alpha-N-acetylgalactosaminidase deficiency type 1
- 3Alpha-N-acetylgalactosaminidase deficiency type 2
- 3Alpha-N-acetylgalactosaminidase deficiency type 3
- 3CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
- 3Carbohydrate deficient glycoprotein syndrome type 1m
- 3Carbohydrate deficient glycoprotein syndrome type 1o
- 3Carbohydrate deficient glycoprotein syndrome type 2a
- 3Carbohydrate deficient glycoprotein syndrome type 2d
- 3Carbohydrate deficient glycoprotein syndrome type 2k
- 3Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency
- 3CCDC115 congenital disorder of glycosylation
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