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- B51836ad401089b36441f96eccbcadda9 hasDbXref "Orphanet:85453" @default.
- B51836ad401089b36441f96eccbcadda9 type Axiom @default.
- B51836ad401089b36441f96eccbcadda9 annotatedProperty IAO_0000115 @default.
- B51836ad401089b36441f96eccbcadda9 annotatedSource MONDO_0010523 @default.
- B51836ad401089b36441f96eccbcadda9 annotatedTarget "X-linked reticulate pigmentary disorder is an extremely rare skin disease described in only four families to date and characterized in males by diffuse reticulate brown hyperpigmentated skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localized brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature." @default.