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HASTALIKLARA GÖRE TESTLER

*Detaylı bilgi için her bir hastalığın üstüne tıklayınız.

*Bizim yapmadığımız testlerin bazılarını çalıştırdığımız, hepsi sertifikalı ve yetkin, tüm yurt dışı ve yurt içi Laboratuvarlar ile anlaşmalıyız. Fiyat indirimi, doku örneklerinin güvenli bir şekilde eldesi, gönderimi ve takibi, testlerin açıklanması ve hastaya genetik danışmanlığının verilmesi tamamen bize ait sorumluluklardır.

*Hastalıklar zaman zaman orijinal, zaman zaman Türkçe isimleriyle dizinlenmiştir. Mümkün olduğunca Türkçe açıklamalara yer verilmeye çalışılmıştır. 

X
Y
Z

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H

Hailey-Hailey disease

Haim-Munk Syndrome

Harlequin Ichthyosis

Hawkinsinuria

Hay-Wells Syndrome

Hearing Loss (İşitme Kaybı)

Hereditary Angioedema (HAE) Type I-II

Hereditary Angioedema (HAE) Type III

Hereditary Fructose Intolerance

Hereditary Hemorrhagic Telangiectasia (HHT)

Hereditary Inclusion Body Myopathy (HIBM)

Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC)

Hereditary Motor and Sensory Neuropathy (HMSN)

Hereditary Multiple Exostoses (HME)

Hereditary Neuropathy with Liability to Pressure Palsy (HNPP)

Hereditary Sensory and Autonomic Neuropathy (HSAN)

Hereditary Sensory and Autonomic Neuropathy I (HSAN I)

Hereditary Sensory and Autonomic Neuropathy II (HSAN II)

Hereditary Sensory and Autonomic Neuropathy III (HSAN III)

Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)

Hereditary Sensory and Autonomic Neuropathy V (HSAN V)

Hereditary Spastic Paraplegia

Herlitz Junctional Epidermolysis Bullosa

Hermansky-Pudlak Syndrome

Heterotaxy

Hidrotic ectodermal dysplasia

Hirschsprung Disease

HMG-CoA Lyase Deficiency

Holocarboxylase Synthetase Deficiency / Multiple Carboxylase Deficiency

Holoprosencephaly

Holt-Oram syndrome

Homocystinuria due to Cystathionine Beta-Synthase Deficiency

HOXD13-Associated Limb Abnormalities

Hoyeraal-Hreidarsson Syndrome (HHS)

HSAN with Spastic Paraplegia

Hydrocephalus, X-linked

Hydroxysteroid (17 Beta) Dehydrogenase 10 Deficiency

Hyper-IgD Syndrome

Hyper-IgE Syndrome (HIES)

Hyperammonemia Due to Carbonic Anhydrase VA Deficiency (CA5AD)

Hyperammonemia Related Disorders

Hyperostosis Corticalis Generalisata, benign form of worth with Torus Palatinus

Hyperparathyroidism-Jaw Tumor Syndrome

Hypertrophic Cardiomyopathy (HCM)

Hypo-/Anhidrotic Ectodermal Dysplasia

Hypocalcemia, Autosomal Dominant (ADH)

Hypochondroplasia (HCH)

Hypogonadotropic Hypogonadism (HH)

Hypohidrotic Ectodermal Dysplasia with Immune Deficiency (HED-ID)

Hypoparathyroidism, sensorineural deafness, and renal disease (HDR)

Hypophosphatemic Rickets, X-linked

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