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Ichthyosis
Informaţii despre
Nume
Ichthyosis
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli fetale
;
Boli genetice
;
Boli rare
Clasificare anatomică Malacards
Boli de piele
Boli din aceeaşi familie
Autosomal Recessive Congenital Ichthyosis
;
Ichthyosis, Acquired
;
Ichthyosis, Congenital, Autosomal Recessive 1
;
Ichthyosis, Congenital, Autosomal Recessive 10
;
Ichthyosis, Congenital, Autosomal Recessive 11
;
Ichthyosis, Congenital, Autosomal Recessive 12
;
Ichthyosis, Congenital, Autosomal Recessive 13
;
Ichthyosis, Congenital, Autosomal Recessive 14
;
Ichthyosis, Congenital, Autosomal Recessive 2
;
Ichthyosis, Congenital, Autosomal Recessive 3
;
Ichthyosis, Congenital, Autosomal Recessive 4a
;
Ichthyosis, Congenital, Autosomal Recessive 4b
;
Ichthyosis, Congenital, Autosomal Recessive 5
;
Ichthyosis, Congenital, Autosomal Recessive 6
;
Ichthyosis, Congenital, Autosomal Recessive 7
;
Ichthyosis, Congenital, Autosomal Recessive 8
;
Ichthyosis, Congenital, Autosomal Recessive 9
Vezi şi
Boli A-Z
Abdominal Wall Defect
Acanthoma
Acute Monoblastic Leukemia
Adenocarcinoma
Aging
Ainhum
Albinism
Alopecia
Alopecia, Androgenetic, 1
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
Alport Syndrome, X-Linked
Al-Raqad Syndrome
Aminoaciduria
Amyloidosis
Anhidrosis
Aniridia 1
Anorexia Nervosa 1
Anosmia
Anterior Cutaneous Nerve Entrapment Syndrome
Arthritis
Arthrochalasia Ehlers-Danlos Syndrome
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Arthrogryposis, Renal Dysfunction, and Cholestasis 1
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Attention Deficit-Hyperactivity Disorder
Autism
Autism X-Linked 2
Autosomal Dominant Progressive External Ophthalmoplegia
Autosomal Recessive Congenital Ichthyosis
Basal Cell Carcinoma
Bazex Syndrome
Biliary Atresia
Blau Syndrome
Blepharoconjunctivitis
Blood Group--Ahonen
Blood Group, I System
Body Mass Index Quantitative Trait Locus 10
Body Mass Index Quantitative Trait Locus 11
Body Mass Index Quantitative Trait Locus 12
Body Mass Index Quantitative Trait Locus 14
Body Mass Index Quantitative Trait Locus 18
Body Mass Index Quantitative Trait Locus 4
Body Mass Index Quantitative Trait Locus 7
Body Mass Index Quantitative Trait Locus 8
Body Mass Index Quantitative Trait Locus 9
Bone Mineral Density Quantitative Trait Locus 15
Bone Mineral Density Quantitative Trait Locus 8
Brachydactyly
Branchiootic Syndrome 1
Burns
Candidiasis
Cataract
Cellulitis
Cerebellar Degeneration
Cerebellar Hypoplasia
Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome
Cerebritis
Cerebro-Oculo-Facio-Skeletal Syndrome
Cervical Rib
Cervicitis
Chanarin-Dorfman Syndrome
Cholangitis
Cholestasis
Chondrodysplasia Punctata 2, X-Linked Dominant
Chondrodysplasia Punctata Syndrome
Chromosome Xp Deletion
Chronic Mucocutaneous Candidiasis
Cicatricial Ectropion
Clear Cell Acanthoma
Coats Disease
Compartment Syndrome
Congenital Disorder of Glycosylation, Type Iq
Congenital Hypothyroidism
Congenital Ichthyosiform Erythroderma
Constrictive Pericarditis
Corneal Degeneration
Corneal Disease
Corneal Dystrophy
Corneal Neovascularization
Cryoglobulinemia
Cutaneous Candidiasis
Cutaneous Mastocytosis
Cutis Laxa
Cutis Laxa, Autosomal Recessive, Type Iiia
Cystinuria
Dermatitis
Dermatitis, Atopic, 2
Dermatophytosis
Dermotrichic Syndrome
Diffuse Cutaneous Mastocytosis
Diffuse Idiopathic Skeletal Hyperostosis
Distal Arthrogryposis
Dominant Ichthyosis Vulgaris
Down Syndrome
Dwarfism
Dysferlinopathy
Dystonia
Ectodermal Dysplasia
Ectropion
Eczema Herpeticum
Endodermal Sinus Tumor
Endometrial Adenocarcinoma
End Stage Renal Failure
Eosinophilic Fasciitis
Epidermodysplasia Verruciformis
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Epidermolytic Acanthoma
Epidermolytic Hyperkeratosis
Epidermolytic Nevus
Epilepsy
Erythroderma, Ichthyosiform, Congenital Reticular
Exfoliative Ichthyosis
Exocrine Pancreatic Insufficiency
Fanconi Syndrome
Fasciitis
Filamentary Keratitis
Fragile X Syndrome
Glomerulonephritis
Granuloma Annulare
Growth Hormone Deficiency
Hansen's Disease
Helix Syndrome
Hepatic Adenomas, Familial
Hepatitis
Histiocytosis
Holocarboxylase Synthetase Deficiency
Hydrops, Lactic Acidosis, and Sideroblastic Anemia
Hyperostosis
Hyperparathyroidism
Hypertrichosis
Hypertrophic Pyloric Stenosis
Hypoglycemia
Hypogonadism
Hypogonadotropic Hypogonadism
Hypogonadotropism
Hypohidrosis
Hypoparathyroidism, Sensorineural Deafness, and Renal Disease
Hypotrichosis
Ichthyosiform Erythroderma, Corneal Involvement, and Deafness
Ichthyosis, Acquired
Ichthyosis Bullosa of Siemens
Ichthyosis--Cheek--Eyebrow Syndrome
Ichthyosis, Congenital, Autosomal Recessive 1
Ichthyosis, Congenital, Autosomal Recessive 11
Ichthyosis, Congenital, Autosomal Recessive 2
Ichthyosis, Congenital, Autosomal Recessive 4a
Ichthyosis, Congenital, Autosomal Recessive 4b
Ichthyosis, Congenital, Autosomal Recessive 7
Ichthyosis Congenita with Biliary Atresia
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
Ichthyosis, Follicular
Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
Ichthyosis Hystrix, Curth-Macklin Type
Ichthyosis Hystrix Gravior
Ichthyosis Lamellar 2
Ichthyosis Lamellar 3
Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis
Ichthyosis Linearis Circumflexa
Ichthyosis Prematurity Syndrome
Ichthyosis Vulgaris
Ichthyosis, X-Linked
Ifap Syndrome with or Without Bresheck Syndrome
Inflammatory Linear Verrucous Epidermal Nevus
Inguinal Hernia
Ischemia
Juvenile Rheumatoid Arthritis
Kagami-Ogata Syndrome
Kallmann Syndrome
Kaufman Oculocerebrofacial Syndrome
Keratitis, Hereditary
Keratosis
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
Kid Syndrome
Leber Congenital Amaurosis
Leber Congenital Amaurosis 5
Lelis Syndrome
Leukemia
Lichen Amyloidosis
Lichen Planus
Lipid Metabolism Disorder
Lipid Storage Disease
Lipodystrophy
Liver Disease
Lung Cancer
Lupus Erythematosus
Lutheran Suppressor, X-Linked
Lymphangiectasis
Lymphatic Malformations
Lymphoblastic Leukemia
Lymphoma
Lymphomatoid Papulosis
Malignant Histiocytosis
Melanoma
Microcephaly
Muckle-Wells Syndrome
Multiple Sulfatase Deficiency
Muscular Dystrophy
Myoclonus
Myopathy
Nail Disorder, Nonsyndromic Congenital, 1
Nephrotic Syndrome
Netherton Syndrome
Neurodegeneration with Brain Iron Accumulation 2a
Neurofibromatosis, Type Ii
Neuronitis
Neuropathy
Nevoid Hypermelanosis, Linear and Whorled
Ocular Albinism
Ocular Motor Apraxia
Oral Squamous Cell Carcinoma
Pachyonychia Congenita 1
Palmoplantar Keratoderma, Nonepidermolytic
Palmoplantar Keratosis
Pancreatitis
Papilloma
Parapsoriasis
Peeling Skin Syndrome
Pellucid Marginal Degeneration
Pericarditis
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial
Peripheral T-Cell Lymphoma
Phelan-Mcdermid Syndrome
Pityriasis Lichenoides
Pityriasis Lichenoides Chronica
Pityriasis Rotunda
Pityriasis Rubra Pilaris
Pneumonia
Poems Syndrome
Polyneuropathy
Pre-Descemet Corneal Dystrophy
Prostatitis
Pseudoainhum
Psoriasis
Psoriasis 13
Pulmonary Alveolar Microlithiasis
Pycnodysostosis
Pyle Disease
Pyloric Stenosis
Quadriplegia
Recessive Dystrophic Epidermolysis Bullosa
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome
Retinitis
Retinitis Pigmentosa
Rhabdomyosarcoma
Rheumatoid Arthritis
Rickets
Rud Syndrome
Sclerosing Cholangitis
Self-Improving Collodion Baby
Sensorineural Hearing Loss
Shwachman-Diamond Syndrome
Sjogren-Larsson Syndrome
Skin Conditions
Skin Disease
Spastic Diplegia
Spasticity
Spastic Quadriplegia
Squamous Cell Carcinoma
Steatorrhea
Sveinsson Chorioretinal Atrophy
Systemic Lupus Erythematosus
Testicular Microlithiasis
Testicular Yolk Sac Tumor
Three M Syndrome 1
Thyroiditis
Tinea Corporis
Transitional Cell Carcinoma
Transmitted_by
Ventricular Septal Defect
Vohwinkel Syndrome
Vohwinkel Syndrome, Variant Form
Wells Syndrome
White Sponge Nevus 1
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