Informaţii despre

Nume Neurofibromatosis, Type Iv, of Riccardi
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Neurofibromatosis (nonmalignant)
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Acanthosis Nigricans Achalasia Achondroplasia Acoustic Neuroma Acromegaly Actinomycosis Acute Lymphocytic Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Adenocarcinoma Adenoiditis Adenoma Adenosquamous Cell Lung Carcinoma Adenosquamous Colon Carcinoma Adermatoglyphia Adie Pupil Adrenal Medulla Cancer Adrenoleukodystrophy Adult Acute Lymphocytic Leukemia Aggressive Digital Papillary Adenocarcinoma Aging Alk-Positive Anaplastic Large Cell Lymphoma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alport Syndrome, X-Linked Al-Raqad Syndrome Amblyopia Amelogenesis Imperfecta Ampulla of Vater Neoplasm Anal Fistula Anaplastic Ganglioglioma Anaplastic Large Cell Lymphoma Andersen Cardiodysrhythmic Periodic Paralysis Aneurysm Angiolipomatosis, Familial Angiomatosis Angioma, Tufted Angiomyolipoma Angiosarcoma Angiosarcoma of the Scalp Aniridia 1 Anisometropia Anorexia Nervosa 1 Antiphospholipid Syndrome Aortic Coarctation Appendix Carcinoid Tumor Arachnoid Cysts Arachnoiditis Aromatase Excess Syndrome Arterial Tortuosity Syndrome Arteriovenous Fistula Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Asplenia, Isolated Congenital Astigmatism Astroblastoma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Telangiectasia Attention Deficit-Hyperactivity Disorder Attenuated Familial Adenomatous Polyposis Atypical Autism Atypical Coarctation of Aorta Atypical Neurofibroma Atypical Polypoid Adenomyoma Atypical Teratoid Rhabdoid Tumor Autism Autism Spectrum Disorder Autosomal Dominant Café Au Lait Spots Autosomal Dominant Disease Autosomal Genetic Disease Back Pain Basal Cell Carcinoma B-Cell Lymphomas Benign Ependymoma Bilateral Breast Cancer Bile Duct Adenocarcinoma Bladder Cancer Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Marrow Cancer Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Stem Glioma Breast Cancer Breast Fibroadenoma Breast Metaplastic Carcinoma Brooke-Spiegler Syndrome Capillary Hemangioma Carcinoid Tumors, Intestinal Cardiofaciocutaneous Syndrome 1 Carney Triad Carpal Tunnel Syndrome Cataract Cauda Equina Syndrome Cavernous Hemangioma Cecum Adenocarcinoma Celiac Disease 1 Cell Type Benign Neoplasm Cellular Schwannoma Central Nervous System Lymphoma Central Precocious Puberty Cerebellar Astrocytoma Cerebellar Hypoplasia Cerebral Aneurysms Cerebritis Cervicitis Charcot-Marie-Tooth Disease Cherubism Chiasmal Syndrome Childhood Kidney Cell Carcinoma Cholestasis Chondroma Chorioretinitis Choroiditis Chromosomal Triplication Chronic Eosinophilic Pneumonia Chronic Inflammatory Demyelinating Polyradiculoneuropathy Coats Disease Cobb Syndrome Colon Adenocarcinoma Colon Adenoma Colorectal Adenocarcinoma Colorectal Adenoma Combined Hamartoma of the Retina and Retinal Pigment Epithelium Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Cone-Rod Dystrophy 2 Congenital Ectropion Uveae Congenital Pseudoarthrosis Congenital Pseudoarthrosis of the Tibia Connective Tissue Disease Constipation Core Binding Factor Acute Myeloid Leukemia Coronary Aneurysm Coronary Artery Aneurysm Coronary Artery Dissection, Spontaneous Cor Triatriatum Cor Triatriatum Dexter Costello Syndrome Cowden Disease Cowden Syndrome 1 Crouzon Syndrome with Acanthosis Nigricans Cystadenoma Cystic Fibrosis Dandy-Walker Syndrome Demodicidosis Desmoid Tumor Desquamative Interstitial Pneumonia Diabetes Insipidus Diabetes Mellitus Diencephalic Syndrome Diffuse Large B-Cell Lymphoma Diverticulitis Down Syndrome Duodenal Somatostatinoma Duodenal Ulcer Duodenitis Duodenum Cancer Dwarfism Dysplastic Nevus Syndrome Dystonia Ectopic Cushing Syndrome Ectropion Elephantiasis Embryonal Rhabdomyosarcoma Empty Sella Syndrome Encephalitis Encephalocele Endocrine Gland Cancer Endometrial Cancer Endotheliitis Enophthalmos Entropion Eosinophilic Pneumonia Ependymoma Epidermodysplasia Verruciformis Epilepsy Epithelioid Malignant Peripheral Nerve Sheath Tumor Epithelioid Sarcoma Equatorial Staphyloma Esotropia Ewing Sarcoma Exocrine Pancreatic Insufficiency Exophthalmos Exostosis Extra-Adrenal Pheochromocytoma Extrahepatic Cholestasis Extraventricular Neurocytoma Familial Adenomatous Polyposis Familial Male-Limited Precocious Puberty Fanconi Anemia, Complementation Group E Fanconi Syndrome Fibromatosis Multiple Non Ossifying Fibromuscular Dysplasia Fibrous Dysplasia Fibrous Histiocytoma Fibrous Meningioma Florid Cemento-Osseous Dysplasia Focal Dystonia Focal Segmental Glomerulosclerosis Foot Drop Foramen Magnum Meningioma Fragile X Syndrome Functioning Pituitary Adenoma Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Gastric Adenocarcinoma Gastric Leiomyosarcoma Gastrinoma Gastroduodenitis Gastrointestinal Stromal Tumor Gastrointestinal System Benign Neoplasm Gastrointestinal System Cancer Giant Cell Glioblastoma Giant Cell Tumor Gigantism Gingivitis Glaucoma 3, Primary Congenital, a Glioblastoma Glioma Gliomatosis Cerebri Gliosarcoma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glomus Tumor Glucose Transporter Type 1 Deficiency Syndrome Goblet Cell Carcinoid Growth Hormone Deficiency Gynecomastia Hansen's Disease Heart Cancer Hemangioblastoma Hemangioma Hemarthrosis Hemidystonia Hemifacial Hyperplasia Hemifacial Spasm Hemimegalencephaly Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatic Angiomyolipoma Hepatitis Hepatoblastoma Hepatocellular Carcinoma Hereditary Paraganglioma-Pheochromocytoma Syndromes Herpes Simplex Hidradenoma Hip Subluxation Histiocytoma Homocystinuria Horseshoe Kidney Hydrocephalus Hydrophthalmos Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperparathyroidism Hyperparathyroidism 2 with Jaw Tumors Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypervitaminosis D Hypoadrenocorticism, Familial Hypopituitarism Hypothalamic Hamartomas Hypotonia Hypotonia-Cystinuria Syndrome Idiopathic Hypercalciuria Immune Suppression Infant Gynecomastia Inflammatory Linear Verrucous Epidermal Nevus Insulinoma Intestinal Benign Neoplasm Intestinal Pseudo-Obstruction Intracranial Hypotension Ischemia Ischemic Retinopathy Juvenile Hereditary Hemochromatosis Juvenile Myelomonocytic Leukemia Juvenile Pilocytic Astrocytoma Juvenile Polyposis Syndrome Juvenile Xanthogranuloma Keloids Kidney Angiomyolipoma Kidney Benign Neoplasm Kidney Cancer Laryngitis Learning Disability Leber Congenital Amaurosis 4 Legius Syndrome Leiomyoma Leiomyomatosis Leiomyosarcoma Lentigines Leopard Syndrome Lepromatous Leprosy Leri-Weill Dyschondrosteosis Leukemia Lichen Nitidus Lichen Sclerosus Linear Scleroderma Lipoprotein Glomerulopathy Liposarcoma Lower Lip Cancer Lung Adenoid Cystic Carcinoma Lung Benign Neoplasm Lung Cancer Lung Disease Lymphangiectasia, Intestinal Lymphangioma Lymph Node Disease Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Lymphoplasmacytic Lymphoma Lynch Syndrome Lynch Syndrome I Macroglossia Macular Dystrophy, Retinal, 1, North Carolina Type Malignant Fibrous Histiocytoma of Bone Malignant Glandular Tumor of Peripheral Nerve Sheath Malignant Peripheral Nerve Sheath Tumor Malignant Triton Tumor Marcus Gunn Phenomenon Marfan Syndrome Mayer-Rokitansky-Kuster-Hauser Syndrome Mccune-Albright Syndrome Mediastinitis Medulloblastoma Megacolon Megalencephaly Meibomian Cyst Melanocytic Nevus Syndrome, Congenital Melanoma Meningeal Melanoma Meningioma, Familial Meningitis Meningocele Meningoencephalocele Meningothelial Meningioma Migraine Without Aura Mismatch Repair Cancer Syndrome Mitochondrial Complex I Deficiency Mitochondrial Complex Ii Deficiency Mixed Cell Type Cancer Mixed Connective Tissue Disease Mn1 Monocytic Leukemia Mononeuritis Multiplex Mononeuropathy Mononeuropathy of the Median Nerve, Mild Monosomy 22 Mosaic Trisomy 8 Moyamoya Disease 1 Mucinous Adenocarcinoma Mucositis 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 Sclerosis Muscular Atrophy Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myeloid Leukemia Myocardial Infarction Myoclonic Epilepsy of Lafora Myoepithelioma Myofibroma Myopathy Myopia Nail-Patella Syndrome Neovascular Glaucoma Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephronophthisis Nephrotic Syndrome Nervous System Cancer Neural Crest Tumor Neuraminidase Deficiency Neurilemmoma Neurilemmomatosis Neuroblastoma Neuroendocrine Tumor Neurofibroma Neurofibroma of Gallbladder Neurofibroma of the Esophagus Neurofibromatosis, Familial Spinal Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type I Neurofibromatosis, Type Ii Neurofibrosarcoma Neuroma Neuronal Intestinal Dysplasia Neuronitis Neuropathy Nevus Anemicus Nevus of Ota Nocardiosis Nodular Hidradenoma Non-Functioning Pituitary Adenoma Noonan Syndrome 1 Obstructive Jaundice Occipital Encephalocele Occipital Neuralgia Oligodendroglioma Oligohydramnios Oncocytoma Oncogenic Osteomalacia Opitz-Kaveggia Syndrome Optic Nerve Glioma Optic Nerve Sheath Meningioma Optic Pathway Glioma Orbital Cancer Orbit Embryonal Rhabdomyosarcoma Organ System Benign Neoplasm Ossifying Fibroma Osteitis Fibrosa Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteofibrous Dysplasia Osteomalacia Ovarian Cyst Paine Syndrome Pancreatic Gastrinoma Pancreatic Islet Cell Tumors Pancreatic Mucinous Cystadenoma Pancreatic Neuroendocrine Tumor Pancreatic Somatostatinoma Pancreatitis Panniculitis Papillary Carcinoma Papilledema Papilloma Paraganglioma Paraganglioma and Gastric Stromal Sarcoma Paragangliomas 1 Parathyroid Adenoma Parathyroid Carcinoma Pectus Carinatum Peptic Ulcer Disease Periampullary Adenocarcinoma Periampullary Adenoma Pericardial Effusion Perineurioma Peripheral Nerve Schwannoma Peripheral Nervous System Neoplasm Persistent Generalized Lymphadenopathy Persistent Hyperplastic Primary Vitreous Peutz-Jeghers Syndrome Phaeochromocytoma Pharyngitis Phelan-Mcdermid Syndrome Pheochromocytoma Pilocytic Astrocytoma Pilomatrixoma Pilomyxoid Astrocytoma Pituitary Hormone Deficiency, Combined, 2 Pleomorphic Liposarcoma Pleomorphic Xanthoastrocytoma Pleuropulmonary Blastoma Plexiform Neurofibroma Plexiform Schwannoma Plexopathy Pneumonia Pneumothorax Polycythemia Polycythemia Vera Polydactyly Polymicrogyria Polyneuropathy Polyradiculoneuropathy Posterior Urethral Valves Posttransplant Acute Limbic Encephalitis Precocious Puberty Primary Ciliary Dyskinesia Primary Congenital Glaucoma Primary Effusion Lymphoma Primary Hyperparathyroidism Primary Optic Atrophy Primary Progressive Multiple Sclerosis Prostatitis Protein-Losing Enteropathy Proteus Syndrome Pseudoangiomatous Stromal Hyperplasia Pseudoarthrosis Pseudohermaphroditism Pseudomyxoma Peritonei Pseudopapilledema Psoriasis Psoriasis 13 Ptosis Pulmonary Embolism Pulmonary Emphysema Pulmonary Hypertension Pulmonary Tuberculosis Pulmonic Stenosis Pulsating Exophthalmos Pure Red-Cell Aplasia Pyoderma Pyoderma Gangrenosum Quadriplegia Radiculopathy Ramer Ladda Syndrome Rectal Neoplasm Refractive Error Renal Hypertension Renovascular Hypertension Reticular Perineurioma Retinal Ischemia Retinitis Retinitis Pigmentosa Retroperitoneal Liposarcoma Rett Syndrome Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Richards-Rundle Syndrome Ring Chromosome 17 Ring Chromosome 22 Rosai-Dorfman Disease Salmonellosis Sarcoma Sarcomatosis Schimmelpenning-Feuerstein-Mims Syndrome Scleral Staphyloma Scoliosis Sebaceous Adenocarcinoma Sebaceous Adenoma Sensorineural Hearing Loss Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Sigmoid Neoplasm Skeletal Dysplasias Skin Benign Neoplasm Sm-Ahnmd Small Intestine Cancer Smith-Kingsmore Syndrome Soft Tissue Sarcoma Somatostatinoma Spasticity Spastic Quadriplegia Spinal Cord Astrocytoma Spinal Cord Ependymoma Spinal Meningioma Spinal Muscular Atrophy Spindle Cell Carcinoma Spiradenoma Splenic Abscess Spondylitis Spondyloarthropathy 1 Spondylocostal Dysostosis 1, Autosomal Recessive Spondylolisthesis Spondylosis Sporadic Pheochromocytoma Squamous Cell Carcinoma Strabismus Struma Ovarii Sturge-Weber Syndrome Subcutaneous Panniculitis-Like T-Cell Lymphoma Subependymal Giant Cell Astrocytoma Subependymoma Subungual Glomus Tumor Superficial Siderosis Superficial Siderosis of the Central Nervous System Sveinsson Chorioretinal Atrophy Syringomyelia Tanycytic Ependymoma Tenosynovial Giant Cell Tumor Teratoma Three M Syndrome 1 Thrombocytosis Thrombosis Thymic Neuroendocrine Tumor Thyroid Cancer Thyroid Carcinoma, Familial Medullary Thyroiditis Tolosa-Hunt Syndrome Tooth Disease Triple X Syndrome Trochlear Nerve Neoplasm Tuberous Sclerosis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Turner Syndrome Ulnar Hypoplasia Undifferentiated Pleomorphic Sarcoma Urethritis Vagus Nerve Neoplasm Vascular Disease Vasoproliferative Tumor of the Retina Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Von Hippel-Lindau Syndrome Vulvar Melanoma Watson Syndrome Wdha Syndrome Weaver Syndrome Weber Syndrome West Syndrome Williams-Beuren Syndrome Wilms Tumor 6 Wilson Disease Wiskott-Aldrich Syndrome Zollinger-Ellison Syndrome