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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Albinism
rdfs:subClassOf
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Albinism
UMLS_CUI
  • C0001916
Contributing_Source
  • NICHD
ALT_DEFINITION
  • A group of genetic conditions marked by little or none of the pigment melanin in the skin, hair, and/or eyes. People with albinism may have vision problems and white or yellow hair; reddish, violet, blue or brown eyes; and pale skin.NCI-GLOSS
FULL_SYN
  • albinismPTNCI-GLOSSCDR0000442860
  • AlbinismPTNCI
  • AlbinismPTNICHD
DEFINITION
  • A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair and skin.NCI
code
  • C84543
http://linked.open...y/mesh/hasConcept
is rdfs:subClassOf of
is sameAs of
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