Informaţii despre

Nume Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Other specified congenital malformation syndromes, not elsewhere classified

Vezi şi

Boli A-Z Adenocarcinoma Adenohypophysitis Adenoma Adenosine Deaminase Deficiency Adult Hepatocellular Carcinoma Alagille Syndrome 1 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Androgen Insensitivity Syndrome Aneurysm Aneurysmal Bone Cysts Angioid Streaks Angiokeratoma Angiomatosis Angiomatous Lymphoid Hamartoma Angiomyolipoma Angiomyomatous Hamartoma Angiosarcoma Aniridia 1 Ankyloglossia Anorexia Nervosa 1 Aortic Coarctation Arachnoid Cysts Arachnoiditis Arteriovenous Fistula Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonitis Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bannayan-Riley-Ruvalcaba Syndrome Basal Cell Carcinoma Basal Cell Nevus Syndrome Basaloid Follicular Hamartoma Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant B-Cell Lymphomas Beckwith-Wiedemann Syndrome Benign Ependymoma Bile Duct Cystadenoma Birt-Hogg-Dube Syndrome Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blue Rubber Bleb Nevus Breast Cancer Breast Disease Bronchial Adenomas/carcinoids Childhood Bronchogenic Cyst Capillary Hemangioma Cardiomyopathy, Infantile Histiocytoid Carney Triad Carpal Tunnel Syndrome Cataract Central Precocious Puberty Cerebellar Hypoplasia Cerebritis Cervical Adenoma Malignum Cervical Mucinous Adenocarcinoma Cervicitis Cholangiocarcinoma Cholelithiasis Chondroma Chordoma Choroiditis Cleft Lip Cloacal Exstrophy Coats Disease Cobb Syndrome Cold-Induced Sweating Syndrome Colitis Colon Adenocarcinoma Combined Hamartoma of the Retina and Retinal Pigment Epithelium Complete Androgen Insensitivity Syndrome Congenital Epulis Congenital Mesoblastic Nephroma Congenital Non-Communicating Hydrocephalus Congenital Pseudoarthrosis Congenital Pseudoarthrosis of the Tibia Congenital Smooth Muscle Hamartoma Conjunctivitis Corneal Dystrophy, Fleck Cowden Disease Cryptogenic Multifocal Ulcerous Stenosing Enteritis Cryptorchidism, Unilateral or Bilateral Cutis Verticis Gyrata Cystadenoma Cystic Kidney Disease Cystic Nephroma Dermatofibrosarcoma Protuberans Dermoid Cyst Diaphragmatic Eventration Diastematomyelia Duodenal Obstruction Duodenal Ulcer Duodenitis Dysplasia Epiphysealis Hemimelica Ectomesenchymoma Embryonal Sarcoma Endotheliitis Enophthalmos Epidermoid Cysts Epignathus Epilepsy Epithelioid Leiomyosarcoma Epulis Estrogen Excess Facial Hemiatrophy Fanconi Anemia, Complementation Group E Fibromatosis Fibrous Dysplasia Focal Cortical Dysplasia, Type Ii Foot Drop Gangliocytoma Ganglioglioma Ganglioneuroma Gastroduodenitis Gastrointestinal Carcinoma Gastrointestinal Stromal Tumor Giant Mammary Hamartoma Gigantism Gigantomastia Gingivitis Gliofibroma Glioma Glomus Tumor Gluteal Muscles, Absence of Growth Hormone Deficiency Gynecomastia Hamartoma, Precalcaneal Congenital Fibrolipomatous Heart Defect, Tongue Hamartoma and Polysyndactyly Hemangioendothelioma Hemangioma Hemangiopericytoma, Malignant Hemifacial Spasm Hemimegalencephaly Hepatic Angiomyolipoma Hepatic Cystic Hamartoma Hepatitis Hepatoblastoma Hereditary Renal Cell Carcinoma Histiocytosis Holoprosencephaly Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperparathyroidism Hyperprolactinemia Hypersomnia Hypersplenism Hypertrichosis Hypohidrosis Hypothalamic Hamartomas Hypotrichosis Infant Gynecomastia Inflammatory Myofibroblastic Tumor Intrahepatic Bile Duct Adenoma Intrahepatic Cholangiocarcinoma Intussusception Inverted Papilloma Islet Cell Tumor Juvenile Nasopharyngeal Angiofibroma Juvenile Pilocytic Astrocytoma Juvenile Polyposis Syndrome Juvenile Xanthogranuloma Kidney Angiomyolipoma Kidney Benign Neoplasm Klippel-Trenaunay-Weber Syndrome Large Cell Carcinoma Laryngitis Leiomyoma Leiomyosarcoma Lennox-Gastaut Syndrome Lentigines Lipomatosis Lipomatosis, Multiple Lissencephaly with Cerebellar Hypoplasia Liver Disease Liver Sarcoma Lobular Neoplasia Lung Cancer Lymphangioleiomyomatosis Lymphangioma Lymphangiomatosis Lymphoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macrodactyly of the Foot Marginal Zone B-Cell Lymphoma Mckusick-Kaufman Syndrome Medulloblastoma Megalencephaly Melanoma Melanotic Neurilemmoma Meningocele Merkel Cell Carcinoma Mesenchymoma Microglandular Adenosis Microphthalmia Microscopic Polyangiitis Mohr Syndrome Mononeuropathy of the Median Nerve, Mild Monosomy 21 Mucositis Multilocular Clear Cell Renal Cell Carcinoma Multilocular Cystic Renal Neoplasm of Low Malignant Potential Myasthenia Gravis Myeloid Sarcoma Myoclonus Myofibroma Myxosarcoma Nasopharyngitis Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuroendocrine Tumor Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuroma Neuronitis Obstructive Hydrocephalus Obstructive Jaundice Odontoma Oligodendroglioma Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex Optic Nerve Hypoplasia, Bilateral Orstavik Lindemann Solberg Syndrome Ossifying Fibroma Osteopetrosis Pallister-Hall Syndrome Pancreatic Islet Cell Tumors Pancreatitis Papilledema Papilloma Peritonitis Peutz-Jeghers Syndrome Pilocytic Astrocytoma Pleuropulmonary Blastoma Plexiform Neurofibroma Pneumothorax Polycystic Liver Disease Polydactyly Polydactyly, Preaxial Iv Polyhydramnios Precocious Puberty Precocious Puberty, Central, 1 Primary Hyperparathyroidism Proteus Syndrome Pseudoangiomatous Stromal Hyperplasia Pseudoarthrosis Pseudopapilledema Pten Hamartoma Tumor Syndrome Pulmonary Coin Lesion Pulmonary Hypertension, Primary, 1 Pulmonary Sclerosing Hemangioma Pustulosis Palmaris Et Plantaris Refractory Anemia Renal Dysplasia Renal Hypoplasia Reproductive Organ Benign Neoplasm Retinitis Retinitis Pigmentosa Rhabdomyomatous Mesenchymal Hamartoma Rhabdomyosarcoma Ruvalcaba Syndrome Sapho Syndrome Sarcoma Sclerosing Hemangioma Scoliosis Seizures, Benign Familial Neonatal, 1 Severe Combined Immunodeficiency Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Sinusitis Skin Lipoma Skin Tag Smooth Muscle Tumor Spindle Cell Hemangioma Spindle Cell Lipoma Spondyloocular Syndrome Steatocystoma Multiplex Sternal Cleft Subependymal Giant Cell Astrocytoma Subependymal Glioma Superficial Siderosis Superficial Siderosis of the Central Nervous System Supernumerary Breasts Syringocystadenoma Papilliferum Teratoma Thyroiditis Tièche-Jadassohn Nevus Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Trichofolliculoma Trigeminal Neuralgia Tuberculous Epididymitis Tuberous Sclerosis Tuberous Sclerosis 1 Turner Syndrome Ulcerative Colitis Undifferentiated Embryonal Sarcoma of the Liver Uterine Benign Neoplasm Verrucous Hemangioma Weber Syndrome Wilms Tumor 6