Informaţii despre

Nume Hemihyperplasia, Isolated
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Congenital malformation syndromes involving early overgrowth

Vezi şi

Boli A-Z Acanthosis Nigricans Acromegaly Adenocarcinoma Adenoma Adrenal Adenoma Adrenal Carcinoma Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenocortical Carcinoma, Hereditary Aggressive Systemic Mastocytosis Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Aniridia 1 Anorexia Nervosa 1 Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ayme-Gripp Syndrome Beckwith-Wiedemann Syndrome Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 Benign Mesenchymoma Beukes Hip Dysplasia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Bornholm Eye Disease Breast Cancer Carpal Tunnel Syndrome Cayler Cardiofacial Syndrome Central Precocious Puberty Cerebritis Chilaiditi Syndrome Chondrosarcoma Chromosomal Triplication Clear Cell Adenocarcinoma Clear Cell Sarcoma Congenital Mesoblastic Nephroma Cowden Syndrome 1 Craniosynostosis 1 Cystathioninuria Embryonal Rhabdomyosarcoma Epilepsy Extraskeletal Mesenchymal Chondrosarcoma Fanconi Anemia, Complementation Group E Fetal Macrosomia Focal Segmental Glomerulosclerosis Folliculitis Gigantism Hallermann-Streiff Syndrome Hemangioblastoma Hemangioendothelioma Hemangioma Hemi 3 Syndrome Hemifacial Hyperplasia Hemimegalencephaly Hepatic Adenomas, Familial Hepatitis Hepatoblastoma Hereditary Wilms' Tumor Hydatidiform Mole, Recurrent, 1 Hydrocephalus Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hypertrichosis Hypomelanotic Disorder Ichthyosis, Congenital, Autosomal Recessive 11 Idiopathic Scoliosis Incontinentia Pigmenti Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Iris Disease Klippel-Trenaunay-Weber Syndrome Leukemia Lipomatosis Lymphangiectasia, Intestinal Lymphangioma Lymphedema Medullary Sponge Kidney Mesenchymal Chondrosarcoma Mesenchymoma Metanephric Adenoma Mononeuropathy of the Median Nerve, Mild Mosaic Trisomy 15 Netherton Syndrome Neurofibromatosis, Type Iv, of Riccardi Nevus, Epidermal Omphalocele Osseous Heteroplasia, Progressive Ovarian Cyst Phacomatosis Pigmentokeratotica Pheochromocytoma Polydactyly Precocious Puberty Protein-Losing Enteropathy Proteus-Like Syndrome Proteus Syndrome Renal Dysplasia Retinal Telangiectasia Retinitis Retroperitoneal Sarcoma Rhabdoid Cancer Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rickets Sarcoma Scoliosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Silver-Russell Syndrome Silver-Russell Syndrome Due to 11p15 Microduplication Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 Silver-Russell Syndrome Due to a Point Mutation Spastic Paraplegia 17, Autosomal Dominant Thymic Hyperplasia Umbilical Hernia Weber Syndrome Whim Syndrome Wilms Tumor 1 Wilms Tumor 5 Wilms Tumor 6 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome Wilson-Turner X-Linked Mental Retardation Syndrome