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MyConsult Provider Profile for Sumit Parikh M.D.
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Sumit Parikh 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)
Cerebellar Degeneration (pediatrics)
Cerebrotendinous Xanthomatosis (pediatrics)
Chronic Progressive External Ophthalmoplegia (pediatrics)
Coenzyme Q10 Deficiency (pediatrics)
Dandy-Walker Syndrome (pediatrics)
Fatty Acid Oxidation Disorder (pediatrics)
Fetal Alcohol Syndrome (pediatrics)
Fragile X (FXS) (pediatrics)
GM1-Gandliosidosis (pediatrics)
GM2-Gandliospdosis (pediatrics)
Genetic Disorder (pediatrics)
Glutaric Acidemia Type I (GA-2) (pediatrics)
Glycine Deficiency (pediatrics)
Glycine N-Methyl Transferase (GNMT) Deficiency (pediatrics)
Holoprosencephaly (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)
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)
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)
Very long-chain acyl-coenzyme A dehydrogenase deficiency (VLCAG) (pediatrics)