Disease: Chromosome 13Q14 Deletion Syndrome

Name
Chromosome 13Q14 Deletion Syndrome
Synonmys
CHROMOSOME 13q DELETION SYNDROME
Classification
developmental, eye, genetic
Associated Genes
-
Mouse Orthologs
-
Source
OMIM:613884 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)

Mouse Models

Learn about how to interpret our results in the Disease Models Help pages

No mouse models associated with OMIM:613884 by orthology to a human gene.

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