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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 F

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
factor XIII deficiency 228500 228500 1
familial dolichocephaly OMIM Home 1
familial epylepsy OMIM Home 12
Fanconi anemia OMIM Home 15
Fanconi anemia, type I *227650 227650 1
Fanconi-Bickel syndrome #227810 227810 2
Farber lipogranulomatosis *228000 228000 2
fibrodysplasia ossificans progressiva *135100 135100 3
fibromatosis, juvenile hyaline *228600 228600 1
Freeman-Sheldon syndrome *193700 193700 2
frontometaphyseal dysplasia *305620 305620 1
fructose intolerance, hereditary *229600 229600 2
fructose-1, 6-diphosphatase deficiency *229700 229700 1
fucosidosis *230000 230000 14

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