Norrie disease

Summary
Synonym
  • Episkopi blindness
  • Norrie-Warburg disease
  • atrophia bulborum hereditaria
Definition
A syndrome characterized by degenerative and proliferative changes of the neuroretina resulting in congenital blindness along with progressive mental disorders in about 50% of patients and sensorineural deafness in about 33% of patients, and that has_material_basis_in mutation in the NDP gene on chromosome Xp11.
Super Class
X-linked recessive disease syndrome
External Links
Disease Ontology
DOID:0060844
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
952 CD38 CD38 molecule
1048 CEACAM5 CEA cell adhesion molecule 5
1087 CEACAM7 CEA cell adhesion molecule 7
55907 CMAS cytidine monophosphate N-acetylneuraminic acid synthetase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024