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bn:01755652n
Noun Concept
Categories: Articles with short description, Disturbances of human pigmentation
EN
X-linked reticulate pigmentary disorder  Amyloidosis, Familial Cutaneous  Familial cutaneous amyloidosis  Partington amyloidosis  Partington cutaneous amyloidosis
EN
X-linked reticulate pigmentary disorder is a rare X-linked genetic condition in which males manifest multiple systemic symptoms and a reticulated mottled brown pigmentation of the skin, which, on biopsy, demonstrated dermal deposits of amyloid. Wikipedia
Definitions
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Sources
EN
X-linked reticulate pigmentary disorder is a rare X-linked genetic condition in which males manifest multiple systemic symptoms and a reticulated mottled brown pigmentation of the skin, which, on biopsy, demonstrated dermal deposits of amyloid. Wikipedia
Rare X-linked genetic condition Wikidata
IS A
disease
rare disease
amyloidosis
skin disease
systemic disease
GENETIC ASSOCIATION
DNA polymerase alpha catalytic subunit
Wikipedia
EN
X-linked reticulate pigmentary disorder
Wikidata
EN
X-linked reticulate pigmentary disorder
Wikipedia Redirections
EN
Familial cutaneous amyloidosis, Partington amyloidosis, Partington cutaneous amyloidosis, Partington syndrome type II, reticulate pigmentary disorder, X-linked reticulate pigmentary disorder with systemic manifestations
Wikidata Alias
EN
Amyloidosis, Familial Cutaneous, Familial cutaneous amyloidosis, Partington disease, PDR, PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS; PDR, X-linked cutaneous amyloidosis, XLPDR

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