help  | about  | cite  | software

Disease :

Primary Identifier  OMIM:261500 Name  EOSINOPHIL PEROXIDASE DEFICIENCY
Paste the following link
Lists
This Disease isn't in any lists. Upload a list.

Function

Disease --> HPO phenotype terms

Genomics

1 Genes

Disease

Disease --> HPO phenotype terms

 

Other

3 Alleles

3 Data Sets

12 Publications





Funding: InterMine has been developed principally through support of the Wellcome Trust. Complementary projects have been funded by the NIH/NHGRI and the BBSRC.

An ELIXIR-UK resource

© 2002 - 2018 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom