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
LE LEA LEB LEC LED LEE LEF LEG LEI LEK LEM LEN LEO LEP LER LES LET LEU LEV LEW LEX LEY
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1. Leo 1031
(UMLS (NCI) C0878090) LEO-1031 =Steroid; Pharmacologic Substance
3. Leontropithecus
[ ] (UMLS (CSP) C0598045) =Mammal ;
2. Leo 275
(UMLS (NCI) C0700708) =Steroid; Pharmacologic Substance
4. LEOPARD syndrome
[An autosomal dominant disorder with an acronym of its seven features (LENTIGO; ELECTROCARDIOGRAM abnormalities; ocular HYPERTELORISM; PULMONARY STENOSIS; abnormal genitalia; retardation of growth; and DEAFNESS or SENSORINEURAL HEARING LOSS). This syndrome is caused by mutations of PTPN11 gene encoding the non-receptor PROTEIN TYROSINE PHOSPHATASE, type 11, and is an allelic to NOONAN SYNDROME. Features of LEOPARD syndrome overlap with those of NEUROFIBROMATOSIS 1 which is caused by mutations in the NEUROFIBROMATOSIS 1 GENES. ( MSH )] (UMLS (CSP) C0175704) =Disease or Syndrome ;

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