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For information, get in touch with: Dott.ssa Barbara Parodi
Email: barbara.parodi@hsanmartino.it
   P. Romano, A. Manniello et al. Nucl Acids Res 2009 37:D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105

Controlled terms of pathologies

Names beginning by N

OMIM(TM), Online Mendelian Inheritance in Man, is a catalog of human genes and genetic disorders authored and edited by Dr. Victor A. McKusick and colleagues at Johns Hopkins and elsewhere. The database contains textual information, pictures, and reference information.

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Pathology nameLink to OMIMNo. of cells
nanism OMIM Home 1
NARP mutation #551500 551500 1
neuraminidase deficiency *256550 256550 9
neuraminidase deficiency with beta-galactosidase deficiency #256540 256540 3
neuroaxonal dystrophy, infantile *256600 256600 1
neurofibromatosis type I *162200 162200 6
neuronal ceroid-lipofuscinosis infantile Finnish type #256730 256730 1
neuropathy, giant axonal *256850 256850 2
Niemann-Pick disease *257200 257200 4
Niemann-Pick disease, type A *257200 257200 30
Niemann-Pick disease, type B *257200 257200 7
Niemann-Pick disease, type C *257220 257220 27

For information, get in touch with:
IRCCS Ospedale Policlinico San Martino
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Barbara Parodi
Email: barbara.parodi@hsanmartino.it

If you want to cite CLDB and HyperCLDB, please use the following reference:

P. Romano, A. Manniello, O. Aresu, M. Armento, M. Cesaro, B. Parodi.
Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines.
Nucleic Acids Research 2009 37(Database issue):D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105