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Meningitis - OMIM - NCBI
Meningitis - OMIM - NCBI
From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
Select item 607115 2.
Cytogenetic locations: 1q44
Select item 613500 3.
Cytogenetic locations: 22q11.23
Select item 613790 4.
Cytogenetic locations: 1p32.2
Select item 610984 5.
Cytogenetic locations: 4q25
Select item 249100 6.
Cytogenetic locations: 16p13.3
Select item 613789 7.
Cytogenetic locations: 1p32.2
Select item 617053 8.
Cytogenetic locations: 7q21.2
Select item 212050 9.
Cytogenetic locations: 9q34.3
Select item 600145 10.
CAUDAL DYSGENESIS SYNDROME, INCLUDED
Cytogenetic locations: 1p13.1
Select item 613002 11.
Cytogenetic locations: 4q35.1
Select item 600802 13.
Cytogenetic locations: 19p13.11
Select item 617900 14.
Cytogenetic locations: 12q14.2
Select item 240500 15.
Cytogenetic locations: 17p11.2
Select item 307200 16.
Cytogenetic locations: Xq22.1
Select item 603553 17.
Cytogenetic locations: 10q22.1
Select item 601457 18.
Cytogenetic locations: 1pter-p36.13, 11p12
Select item 209920 19.
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A, INCLUDED
Cytogenetic locations: 1pter-p36.13, 13q13.3, 1pter-p36.13, 1q21.3
Select item 267700 20.
Cytogenetic locations: 9q21.3-q22
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