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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
L L L- L0 L1 L6 LA LB LC LD LE LF LG LH LI LK LL LM LN LO LP LR LS LT LU LV LX LY
LA LAB LAC LAD LAE LAF LAG LAJ LAK LAL LAM LAN LAP LAR LAS LAT LAU LAV LAW LAX LAY

Laurence Moon Biedl 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) ( MSH )]
UMLS (CSP) C0023138
 
Congenital Abnormality
Disease or Syndrome
Relation/PAR: Abnormalities, Multiple
Hypothalamic Diseases

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