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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 H

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
hair - brain syndrome *234050 234050 2
Hallervorden-Spatz disease *234200 234200 1
hemochromatosis neonatal #231100 231100 1
hereditary emphysema OMIM Home 1
hermaphroditism true 235600 235600 5
histiocytosis X *235900 235900 1
homocystinuria *236200 236200 6
homocystinuria - megaloblastic anemia *236270 236270 7
Huntington chorea *143100 143100 1
hydrocephalus 236600 236600 2
hydrocephalus, agyria, retinal dysplasia Hard syndrome/Walker-Warburg *236670 236670 1
hyperammonemia due to carbamoylphosphate synthetase deficien. 237300 237300 1
hypercholesterolemia, familial *143890 143890 158
hyperglycerolemia *307030 307030 1
hyperglycinemia, nonketotic #605899 605899 3
hyperlipoproteinemia I *238600 238600 1
hypophosphatasia infantile #241500 241500 1

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