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Congenital Stationary Night Blindness
Informaţii despre
Nume
Congenital Stationary Night Blindness
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli genetice
;
Boli rare
Clasificari ICD10
Night blindness
Clasificare anatomică Malacards
Boli ale ochiului
Boli din aceeaşi familie
Autosomal Dominant Congenital Stationary Night Blindness
;
Autosomal Recessive Congenital Stationary Night Blindness
;
Night Blindness, Congenital Stationary, Autosomal Dominant 1
;
Night Blindness, Congenital Stationary, Autosomal Dominant 2
;
Night Blindness, Congenital Stationary, Autosomal Dominant 3
;
Night Blindness, Congenital Stationary, Type 1a
;
Night Blindness, Congenital Stationary, Type 1b
;
Night Blindness, Congenital Stationary, Type 1c
;
Night Blindness, Congenital Stationary, Type 1d
;
Night Blindness, Congenital Stationary, Type 1e
;
Night Blindness, Congenital Stationary, Type 1f
;
Night Blindness, Congenital Stationary, Type 1g
;
Night Blindness, Congenital Stationary, Type 1h
;
Night Blindness, Congenital Stationary, Type 2a
Vezi şi
Boli A-Z
Achromatopsia
Achromatopsia 3
Adie Pupil
Aland Island Eye Disease
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
Al-Raqad Syndrome
Aniridia 1
Anorexia Nervosa 1
Arthrochalasia Ehlers-Danlos Syndrome
Autosomal Dominant Congenital Stationary Night Blindness
Autosomal Recessive Congenital Stationary Night Blindness
Blood Group--Ahonen
Blood Group, Dombrock System
Choroideremia
Chromosome 15q13.3 Deletion Syndrome
Cone Dystrophy
Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 3
Cone-Rod Dystrophy 6
Degeneration of Macula and Posterior Pole
Focal Chorioretinitis
Fundus Albipunctatus
Hepatic Adenomas, Familial
Hereditary Night Blindness
Hereditary Retinal Dystrophy
Keratoconus
Keratomalacia
Leber Congenital Amaurosis
Leber Congenital Amaurosis 1
Leber Congenital Amaurosis 12
Leber Congenital Amaurosis 4
Leber Congenital Amaurosis 9
Melanoma-Associated Retinopathy
Muscular Dystrophy
Myopia
Night Blindness
Night Blindness, Congenital Stationary, Autosomal Dominant 2
Night Blindness, Congenital Stationary, Type 1a
Night Blindness, Congenital Stationary, Type 1b
Night Blindness, Congenital Stationary, Type 1e
Night Blindness, Congenital Stationary, Type 2a
Prolonged Electroretinal Response Suppression
Red-Green Color Blindness
Retinal Degeneration
Retinal Disease
Retinitis
Retinitis Pigmentosa
Retinitis Pigmentosa 26
Retinitis Pigmentosa 3
Retinoschisis 1, X-Linked, Juvenile
Rhyns Syndrome
Scotoma
Severe Early-Childhood-Onset Retinal Dystrophy
Stargardt Disease
Stargardt Disease 1
Stargardt Macular Degeneration
Strabismus
Usher Syndrome, Type Iid
Van Der Woude Syndrome 1
X-Linked Congenital Stationary Night Blindness
Yemenite Deaf-Blind Hypopigmentation Syndrome
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