reticulate acropigmentation of kitamura Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pigmentation disease characterized by lesions that initially arise as letiginous, hyperpigmented macules in a reticular pattern on the dorsal aspect of the hands and feet. Over time, lesions may spread proximally and may darken; palmoplantar pitting and dermatoglyphic disruption may also be present. (Human Disease Ontology, DOID_0060258)
External Link http://www.omim.org/entry/615537
Similar Terms
Downloads & Tools

Genes

1 genes associated with the reticulate acropigmentation of kitamura phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10