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AttributesValues
rdf:type
rdfs:label
  • Laurence-Moon Syndrome
rdfs:subClassOf
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Laurence-Moon Syndrome
UMLS_CUI
  • C0023138
ALT_DEFINITION
  • An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9)MSH2003_2003_05_12
Legacy_Concept_Name
  • Laurence-Moon_Syndrome
FULL_SYN
  • Laurence-Moon SyndromePTNCI
code
  • C34760
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