Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
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Preferred Name

Mannosidase Deficiency Diseases
Synonyms

Mannosidase Deficiency Disease
Definitions

Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
ID

http://purl.bioontology.org/ontology/MESH/D044904
altLabel

Mannosidase Deficiency Disease

Diseases, Mannosidase Deficiency

Mannosidase Deficiency Syndrome

Deficiency Disease, Mannosidase

Mannosidase Deficiency Syndromes

Mannosidosis

Deficiency Syndromes, Mannosidase

Deficiency Syndrome, Mannosidase

Mannosidoses

Deficiency Diseases, Mannosidase
AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui

C1257960
DC

1
definition

Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
DX

20040101
FX

D008361
HN

2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469
Inverse of RO

http://purl.bioontology.org/ontology/MESH/D008361
Machine permutation

2004; see MANNOSIDOSIS 1984-2003
MDA

20030709
MMR

20130708
MN

C18.452.648.202.607

C18.452.648.595.577

C16.320.565.202.607

C16.320.565.595.577
notation

D044904
prefLabel

Mannosidase Deficiency Diseases
TERMUI

T024887

T534623

T534622
TH

NLM (2004)

NLM (1985)

GHR (2014)
tui

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D016464

http://purl.bioontology.org/ontology/MESH/D002239
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http://purl.bioontology.org/ontology/ICD10CM/E77.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI