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WormBase Tree Display for DO_term: DOID:0111834

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Name Class

DOID:0111834NameX-linked reticulate pigmentary disorder
StatusValid
DefinitionA 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.
SynonymExactPDR
Partington disease
X-linked reticulate pigmentary disorder with systemic manifestations
ParentIs_aDOID:10123
DOID:0050735
DB_infoDatabaseOMIMdisease301220
Attribute_ofGene_by_orthologyWBGene00012936