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MyConsult Provider Profile for Manikum Moodley M.D.
Provider Profile

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Manikum Moodley M.D.

Below is a list of conditions that this physician provides for online medical second opinions. Please understand that we cannot guarantee that this requested physician will be available to provide the second opinion. However, we will do our best to accomodate your request for the physician of your choice.

To begin the online medical second opinion process, please click on the name of the condition below for which you are requesting an online second opinion.

Adrenoleukodystrophy (pediatrics)
Adrenomyeloneuropathy (AMN) (pediatrics)
Aneuploidy (pediatrics)
Battens Disease (pediatrics)
Canavan Disease (pediatrics)
Carnitine Deficiency (pediatrics)
Cerebrotendinous Xanthomatosis (pediatrics)
Chronic Progressive External Ophthalmoplegia (pediatrics)
Coenzyme Q10 Deficiency (pediatrics)
Craniosynostosis (pediatrics)
Dandy-Walker Syndrome (pediatrics)
Deletion 22q11 Syndrome (pediatrics)
Developmental Delay (pediatrics)
Duplication 10q Syndrome (pediatrics)
Eaton-Lambert Syndrome (LEMS) (pediatrics)
Fabry Disease (pediatrics)
Fatty Acid Oxidation Disorder (pediatrics)
Fetal Alcohol Syndrome (pediatrics)
Fragile X (FXS) (pediatrics)
Fragile X-associated premature ovarian failure (POF) (pediatrics)
Fragile X-associated tremor/ataxia syndrome (FXTAS) (pediatrics)
GM1-Gandliosidosis (pediatrics)
GM2-Gandliospdosis (pediatrics)
Gaucher's Disease (pediatrics)
Genetic Disorder (pediatrics)
Glutaric Acidemia (pediatrics)
Glutaric Acidemia Type I (GA-2) (pediatrics)
Glutaric Acidemia Type I (GA-I) (pediatrics)
Glycine Deficiency (pediatrics)
Glycine N-Methyl Transferase (GNMT) Deficiency (pediatrics)
Holoprosencephaly (pediatrics)
Huntington Disease (pediatrics)
Hypotonia (pediatrics)
Isovaleric Acidemia (IVA) (pediatrics)
Kearn Sayre Syndrome (pediatrics)
Kuff's Disease (pediatrics)
Leigh Disease (pediatrics)
Lesch-Nyhan Syndrome (LNS) (pediatrics)
Leukodystrophy (pediatrics)
Lipid Storage Disease (pediatrics)
Long-Chain 3 Hydroxyacyl CoA Dehydrogense (LCHAD) (pediatrics)
Lysosomal Storage Disease (pediatrics)
MELAS Syndrome (pediatrics)
Medium Chain acyl CoA Dehydrogenase (MCAD) (pediatrics)
Menkes Disease (pediatrics)
Mental Retardation (pediatrics)
Mitochondrial Disease (pediatrics)
Myoclonus Epilepsy Associated with Ragged-Red Fibers (pediatrics)
Neurodegeneration Disease (pediatrics)
Neuronal Ceroid Lipofuscinoses (pediatrics)
Neurotransmitter Disease (pediatrics)
Neurotransmitter Syndrome (pediatrics)
Niemann Pick Disease (pediatrics)
Ophthalmoplegia (pediatrics)
POLG1 (pediatrics)
Paraneoplastic Cerebellar Degeneration (PCD) (pediatrics)
Parkinson's Disease (pediatrics)
Peroxisomal Disease (PSD) (pediatrics)
Propionic Acidemia (PROP) (pediatrics)
Retinitis Pigmentosa (pediatrics)
Rett Syndrome (pediatrics)
Sandhoff Disease (pediatrics)
Spinocerebellar Atrophy (pediatrics)
Tay-Sachs Disease (pediatrics)
Trisomy (pediatrics)
Turner Syndrome (pediatrics)
Very long-chain acyl-coenzyme A dehydrogenase deficiency (VLCAG) (pediatrics)