Provider Name
Service provider

Your Medical Gate - Al Naeim

Showing 316 to 336 of 597 entries
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Tests

Transferrin Saturation Ratio

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Congenital Adrenal hyperplasia (CYP21A2 21-hydroxy

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Anti Myeloperoxidase Abs (MPO)

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Cornelia-De-Lange syndrome Panel (HDAC8, NIPBL, RA

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Multiple joint dislocations, short stature, cranio

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Craniofacial and neuro-developmental abnormalities

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Fanconi anemia Panel (BRCA2, BRIP1, FANCA, FANCB,

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frontometaphyseal dysplasia (FLNA) Sequencing

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Fructose-1,6-bisphosphatase deficiency (FBP1) Sequ

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Fructose-1,6-bisphosphatase deficiency (FBP1) Dele

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Galactosemia (GALT) Sequencing

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Gaucher disease (GBA) Sequencing

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Glycogen storage diseases Basic Panel (G6PC, SLC37

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Deafness, non-syndromic sensorineural autosomal re

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Deafness, non-syndromic sensorineural autosomal do

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Joubert syndrome gene Panel (26 genese) sequencing

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Joubert syndrome gene Panel (26 genese) by Deletio

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Mitochondrial diseases gene Panel (22 genesf) sequ

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Mitochondrial diseases gene Panel (22 genesf) by D

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Hypoparthyroidism-retardation-dysmorphism (Sanjad-

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AIRE gene (Autoimmune polyendocrinopathy syndrome

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