Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

COMPLEMENT COMPONENT 5 DEFICIENCY
Synonyms

C5D
ID

http://purl.bioontology.org/ontology/OMIM/609536
altLabel

C5D

C5 DEFICIENCY
cui

C0343047
Gene Locus

9q34.1
Gene Symbol

C5D

ECLZB

C5
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

609536
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

COMPLEMENT COMPONENT 5 DEFICIENCY
tui

T047
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http://purl.obolibrary.org/obo/DOID_8158 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/MESH/C537005 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C537005 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/ICD10/L21.1 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10CM/L21.1 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bmicc.cn/ontology/ICD10CN/L21.1 International Classification of Diseases, 10th Edition, China CUI