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Laurence-Moon-Biedl-Bardet syndrome. 1985

N N Laha, and V N Mishra, and B Shukla, and A Shanker

UI MeSH Term Description Entries
D007849 Laurence-Moon Syndrome 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) Laurence-Moon-Biedl Syndrome,Laurence Moon Biedl Syndrome,Laurence Moon Syndrome,Syndrome, Laurence-Moon,Syndrome, Laurence-Moon-Biedl
D008297 Male Males
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

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