RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: meningococcal meningitis
Accession: DOID:0080176
browse the term
Definition: A bacterial meningitis that has_material_basis_in Neisseria meningitidis infection. (DO)
Synonyms: exact_synonym: meningococcic meningitis
narrow_synonym: meningococcal meningitis, serogroup C; meningococcal meningitis, serogroup A; meningococcal meningitis, serogroup B; meningococcal meningitis, serogroup W 135; meningococcal meningitis, serogroup W135; meningococcal meningitis, serogroup Y
primary_id: MESH:D008585
xref: EFO:1001040 ; ICD10CM:A39.0 ; ICD9CM:036.0
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C9
complement C9
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:9570574
NCBI chr16:24,521,318...24,575,939
Ensembl chr16:24,520,634...24,590,338
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CD46
CD46 molecule, complement regulatory protein
ISO
RGD
PMID:12869763
RGD:6483466
NCBI chr 9:135,025,439...135,078,910
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CFP
complement factor properdin
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:8530058 PMID:10909851
NCBI chr X:42,145,754...42,152,879
Ensembl chr X:42,143,697...42,152,868
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MARCO
macrophage receptor with collagenous structure
ISO
protein:increased expression:sub-cortical, meninges, astrocyte
RGD
PMID:21299846
RGD:41412190
NCBI chr15:24,502,935...24,541,286
Ensembl chr15:24,503,108...24,541,283
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MMP13
matrix metallopeptidase 13
ISO
RGD
PMID:10430840
RGD:8547971
NCBI chr 9:33,549,003...33,616,700
Ensembl chr 9:33,549,008...33,561,162
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MMP9
matrix metallopeptidase 9
ISO
RGD
PMID:10430840
RGD:8547971
NCBI chr17:48,179,690...48,186,782
Ensembl chr17:48,179,671...48,186,788
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NOD2
nucleotide binding oligomerization domain containing 2
susceptibility
ISO
DNA:SNP,haplotype: :SNP8(human)
RGD
PMID:23691182
RGD:7800668
NCBI chr 6:34,132,127...34,167,446
Ensembl chr 6:34,130,938...34,177,534
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SLC11A1
solute carrier family 11 member 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:16597321
NCBI chr15:120,434,100...120,446,396
Ensembl chr15:120,433,952...120,446,396
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TLR2
toll like receptor 2
susceptibility
ISO
DNA:haplotype: :2477G>A(rs5743708)(human)
RGD
PMID:23691182
RGD:7800668
NCBI chr 8:75,416,257...75,428,370
Ensembl chr 8:75,411,993...75,428,330
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TLR4
toll like receptor 4
susceptibility
ISO
DNA:SNP,haplotype: :896A>G(rs4986790)(human)
RGD
PMID:23691182
RGD:7800668
NCBI chr 1:258,044,610...258,054,641
Ensembl chr 1:258,044,610...258,058,970
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