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Disease Ontology Browser
X-linked reticulate pigmentary disorder (DOID:0111834)
Alliance: disease page
Synonyms: Partington disease; X-linked reticulate pigmentary disorder with systemic manifestations
Alt IDs: OMIM:301220, MESH:C564461, ORDO:85453, UMLS_CUI:C1845050
Definition: A pigmentation disease characterized by early onset of recurrent respiratory infections, failure to thrive resulting from inflammatory gastroenteritis or colitis, and reticular pigmentation abnormalities of the skin in hemizygous males and only pigmentary abnormalities along the lines of Blaschko in heterozygous females that has_material_basis_in mutation in the POLA1 gene on chromosome Xp22.1-p21.3.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory