ML

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ML

The two-character ISO 3166 country code for MALI.
Copyright © 2012, Campbell R. Harvey. All Rights Reserved.

ML

1. See Merrill Lynch and Co.

2. ISO 3166-1 alpha-2 code for the Republic of Mali. This is the code used in international transactions to and from Malian bank accounts.

3. ISO 3166-2 geocode for Mali. This is used as an international standard for shipping to Mali. Each Malian region has its own code with the prefix "ML" and a number following. For example, the code for the Region of Gao is ISO 3166-2:ML-7. The city of Bamako has its own lettered designation: ISO 3166-2:ML-BKO.
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References in periodicals archive ?
Mucolipidosis type III in an adolescent presenting with atypical facial features and skeletal deformities.
(1,4,11,12) Mucolipidosis type II [alpha]/[beta] and ML III [alpha]/[beta], the principal focus of the current report, are the result of mutations in the gene coding for the [alpha]/[beta] subunit where the catalytic domain resides.
Mucolipidosis II: This syndrome, also known as i cell disease, is characterized by short stature, coarse facial features, psychomotor retardation and gingival enlargement.
[1] Nonstandard abbreviations: MPS, mucopolysaccharidosis; MLP, mucolipidosis; DBFP, dried blood spots on filter paper; and 4MU, 4 methylumbelliferyl.
Among the LSD-affected individuals, all individuals with acid lipase deficiency and 86%, 60%, and 58% of individuals with mucolipidosis II/III, Niemann-Pick (A/B) disease, and Gaucher disease, respectively, had total acid [alpha]-glucosidase concentrations higher than the 95th percentile of the control group (Table 1).
Palmdale, CA 93551 (805) 267-2570 (voice/fax) ??lorit@netport..com http://www.wincom.net/moebius/ 1,2,3,6,8,9 MONOSOMY X See: Turner Syndrome MORQUIO SYNDROME See: Mucopolysaccharidosis; Tay-Sachs Disease MORVAN DISEASE See: Syringomyelia MOTOR-SENSORY NEUROPATHY, HEREDITARY See: Charcot-Marie-Tooth Disease MOYAMOYA DISEASE See: Stroke; Vascular Malformations Families with Moyamoya Network c/o Dawn Gruettner 4900 McGowan St., SE Cedar Rapids, IA 52403 (800) 261-6692 2,3 MUCOLIPIDOSES See: Mucopolysaccharidosis; Mucolipidosis Type IV; Tay-Sachs Disease MUCOLIPIDOSIS TYPE IV See also: Mucopolysaccharidosis; Tay-Sachs Disease; Visual Impairments ML4 Foundation 719 East 17th St.
It is worth noting that 13 of the LSD plasma samples were from newborns (<6 weeks of age), representing Gaucher (n = 3), Krabbe (n = 1), MLD (n = 2), MPS VI (n = 2), mucolipidosis II/III (n = 1), Niemann-Pick C (n = 2), Pompe (n = 1), and Tay-Sachs (n = 1) disorders.
SE Cedar Rapids, IA 52403 (800) 261-6692 2,3 MUCOLIPIDOSES See: Mucopolysaccharidosis; Mucolipidosis Type IV; Tay-Sachs Disease MUCOLIPIDOSIS TYPE IV See: Mucopolysaccharidosis; Tay-Sachs Disease; Visual Impairments ML4 Foundation 719 E.
I-Cell disease (mucolipidosis II, McKusick 252500) and a clinically milder, form pseudo-Hurler polydystrophy (mucolipidosis III, McKusick 252600), are autosomal, recessively inherited lysosomal storage diseases in which the transport of newly synthesized lysosomal enzymes into lysosomes is affected (6).
At 5:03 PM, August 16, 1990, my husband, David, phoned to tell me ' that our son, Scott, had a rare metaboric disease called Mucolipidosis Type IV or ML4.
Visualization of storage vacuoles by electron microscopy has also been proposed as a method for prenatal diagnosis of mucolipidosis [34].
See: Mucolipidosis Type IV, Mucopolysaccharidosis, Tay-Sachs Disease