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Autosomal Genetic Disease
Informaţii despre
Nume
Autosomal Genetic Disease
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli genetice
Vezi şi
Boli A-Z
Acrofacial Dysostosis
Actinic Cheilitis
Adenoma
Adenosquamous Colon Carcinoma
Aging
Alpha-Thalassemia
Amyloid Tumor
Anal Fistula
Appendix Carcinoid Tumor
Arthrochalasia Ehlers-Danlos Syndrome
Astrocytoma
Attenuated Familial Adenomatous Polyposis
Atypical Polypoid Adenomyoma
Atypical Werner Syndrome
Autosomal Dominant Disease
Autosomal Dominant Limb-Girdle Muscular Dystrophy
Autosomal Dominant Polycystic Kidney Disease
Bardet-Biedl Syndrome 17
Beta-Thalassemia
Birt-Hogg-Dube Syndrome
Brain Cancer
Breast Papillary Carcinoma
Calcifying Epithelial Odontogenic Tumor
Caroli Disease
Cecal Benign Neoplasm
Cecum Adenocarcinoma
Cell Type Benign Neoplasm
Cellular Schwannoma
Cerebral Aneurysms
Cerebral Convexity Meningioma
Cerebro-Oculo-Facio-Skeletal Syndrome
Childhood Kidney Cell Carcinoma
Choroid Plexus Cancer
Cockayne Syndrome
Cockayne Syndrome B
Colonic Benign Neoplasm
Colorectal Adenocarcinoma
Colorectal Adenoma
Colorectal Cancer
Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly
Congenital Hemolytic Anemia
Congenital Hepatic Fibrosis
Cowden Disease
Cystic Fibrosis
Cystic Kidney Disease
Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 6
Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 16
Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct
Diffuse Gastric Cancer
Elephantiasis
Endometrial Adenocarcinoma
Endometrial Cancer
Familial Adenomatous Polyposis
Familial Colorectal Cancer
Familial Renal Oncocytoma
Familial Renal Papillary Carcinoma
Female Reproductive Organ Cancer
Fetal Hemoglobin Quantitative Trait Locus 1
Gastric Cancer
Gastric Leiomyoma
Gastrointestinal System Benign Neoplasm
Gastrointestinal System Cancer
Gliofibroma
Hemoglobin C Disease
Hemoglobin D Disease
Hemoglobin E Disease
Hemoglobin H Disease
Hemoglobin Lepore-Beta-Thalassemia Syndrome
Hemoglobinopathy
Hepatic Adenomas, Familial
Hereditary Breast Ovarian Cancer Syndrome
Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome
Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome
Hereditary Renal Cell Carcinoma
Hormone Producing Pituitary Cancer
Hyperparathyroidism
Hyperparathyroidism 2 with Jaw Tumors
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertension, Essential
Hypophosphatemic Bone Disease
Integumentary System Cancer
Intestinal Benign Neoplasm
Jejunal Cancer
Keratoacanthoma
Kidney Angiomyolipoma
Kidney Cancer
Legius Syndrome
Li-Fraumeni Syndrome
Lip Cancer
Lipomatosis
Lower Lip Cancer
Lung Disease
Lung Papillary Adenocarcinoma
Lymphatic Malformations
Lynch Syndrome
Lynch Syndrome I
Malignant Peripheral Nerve Sheath Tumor
Malignant Secondary Hypertension
Melanocytic Nevus Syndrome, Congenital
Melanotic Neurilemmoma
Meningioma, Radiation-Induced
Mid-Dermal Elastolysis
Mismatch Repair Cancer Syndrome
Muir-Torre Syndrome
Multiple Endocrine Neoplasia
Multiple Endocrine Neoplasia Type 1 and Type 2
Multiple Endocrine Neoplasia, Type I
Multiple Endocrine Neoplasia, Type Iia
Multiple Endocrine Neoplasia, Type Iib
Multiple Endocrine Neoplasia, Type Iv
Multiple Self-Healing Squamous Epithelioma
Mutagen Sensitivity
Mutyh-Associated Polyposis
Nervous System Cancer
Neurilemmoma
Neurilemmomatosis
Neurofibromatosis, Familial Spinal
Neurofibromatosis, Type Iv, of Riccardi
Neurofibrosarcoma
Olfactory Groove Meningioma
Optic Nerve Neoplasm
Organ System Benign Neoplasm
Osgood-Schlatter's Disease
Pancreatic Islet Cell Tumors
Peutz-Jeghers Syndrome
Pheochromocytoma
Plexiform Neurofibroma
Polycystic Kidney Disease
Polycystic Kidney Disease 1
Polycystic Kidney Disease 2
Polycystic Kidney Disease 3
Polycystic Kidney Disease 4 with or Without Hepatic Disease
Polycystic Kidney Disease 5
Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis
Polycystic Liver Disease
Polycystic Liver Disease 1
Polyposis Syndrome, Hereditary Mixed, 1
Primary Hyperparathyroidism
Primary Peritoneal Carcinoma
Pseudoxanthoma Elasticum
Pten Hamartoma Tumor Syndrome
Rectal Neoplasm
Renal-Hepatic-Pancreatic Dysplasia
Sebaceous Adenocarcinoma
Sebaceous Adenoma
Sensorineural Hearing Loss
Sickle Cell Disease
Skin Benign Neoplasm
Small Intestine Cancer
Spinal Cancer
Spinal Cord Ependymoma
Spinal Meningioma
Sporadic Breast Cancer
Thalassemia
Thyroid Cancer, Nonmedullary, 1
Trichothiodystrophy 1, Photosensitive
Tricuspid Valve Prolapse
Tuberous Sclerosis
Usher Syndrome, Type Id
Von Hippel-Lindau Syndrome
Xeroderma Pigmentosum, Complementation Group B
Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group F
Xeroderma Pigmentosum, Complementation Group G
Xeroderma Pigmentosum, Variant Type
Xfe Progeroid Syndrome
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