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Nume Growth Hormone Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli endocrine

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Boli A-Z Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acid-Labile Subunit Deficiency Acromegaly Acth Deficiency, Isolated Adenoma Adrenal Gland Hyperfunction Adrenal Hypoplasia, Congenital Afibrinogenemia, Congenital Agammaglobulinemia Aging Alopecia Alopecia Areata Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Amenorrhea Androgen Insensitivity Syndrome Aniridia 1 Anorexia Nervosa 1 Arachnoid Cysts Arachnoiditis Argininemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Telangiectasia Atherosclerosis Susceptibility Autoimmune Polyglandular Syndrome Type 3 Basal Encephalocele Blood Group--Ahonen Blood Group, Dombrock System 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 Borjeson-Forssman-Lehmann Syndrome Brachydactyly Brain Injury Brain Tumor, Childhood Bulimia Nervosa 2 Cataract Cat Eye Syndrome Central Precocious Puberty Central Sleep Apnea Cerebral Palsy Cerebritis Choroiditis Chromosome 16p13.3 Deletion Syndrome, Proximal Cleft Lip Cleft Lip/palate Cleft Lip/palate with Abnormal Thumbs and Microcephaly Cockayne Syndrome Cockayne Syndrome a Cohen Syndrome Combined Pituitary Hormone Deficiencies, Genetic Forms Combined Pituitary Hormone Deficiency Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conduct Disorder Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Microgastria Congenital Rubella Costello Syndrome Craniopharyngioma Crouzon Syndrome Cutis Laxa, Autosomal Recessive, Type Iiia Cystic Fibrosis Cystinuria Dermatomyositis Desbuquois Dysplasia Dextrocardia Diabetes Insipidus Diabetes Mellitus Diencephalic Syndrome Diffuse Idiopathic Skeletal Hyperostosis Dilated Cardiomyopathy Donohue Syndrome Duane Retraction Syndrome Dubowitz Syndrome Dwarfism Eating Disorder Empty Sella Syndrome Encephalocele Encephalocraniocutaneous Lipomatosis Encephalomyopathy Encephalopathy Endotheliitis Epilepsy Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasting Hypoglycemia Fibromatosis Multiple Non Ossifying Floating-Harbor Syndrome Focal Segmental Glomerulosclerosis Frontonasal Dysplasia 1 Functioning Pituitary Adenoma Ganglioneuroblastoma Gaucher Disease, Type I Gigantism Gilles De La Tourette Syndrome Gitelman Syndrome Glucocorticoid Resistance, Generalized Glycogen Storage Disease Gonadal Dysgenesis Growth Control, Y-Chromosome Influenced Growth Hormone Insensitivity, Partial Growth Hormone Secreting Pituitary Adenoma Hajdu-Cheney Syndrome Helix Syndrome Hepatic Adenomas, Familial Hepatitis Hereditary Multiple Exostoses Human Coronavirus Sensitivity Hydrocephalus Hyperinsulinism Hyperparathyroidism Hyperpituitarism Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypoadrenocorticism, Familial Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypoparathyroidism Hypopituitarism Hypothalamic Disease Hypothalamic Hamartomas Hypothyroidism, Congenital, Nongoitrous, 4 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function Ichthyosis Immunoglobulin Alpha Deficiency Infertility Inflammatory Bowel Disease Insulin-Like Growth Factor I Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Ia Isolated Growth Hormone Deficiency, Type Ib Isolated Growth Hormone Deficiency, Type Ii Isolated Growth Hormone Deficiency, Type Iii Jacobsen Syndrome Juvenile Rheumatoid Arthritis Kearns-Sayre Syndrome Lactic Acidosis Laron Syndrome Laryngeal Cleft Leber Congenital Amaurosis 4 Leigh Syndrome Leukemia Lipodystrophy Lipomatosis Lymphoblastic Leukemia Lymphocytic Choriomeningitis Lysinuric Protein Intolerance Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Marasmus Megaesophagus Megalencephaly Melnick-Needles Syndrome Meningitis Meningoencephalitis Microphthalmia Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mixed Gonadal Dysgenesis Morning Glory Syndrome Mulibrey Nanism Muscular Dystrophy Myelomeningocele Myopathy Netherton Syndrome Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuropathy Nonalcoholic Steatohepatitis Non-Functioning Pituitary Adenoma Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 Nutritional Deficiency Disease Occipital Horn Syndrome Oliver-Mcfarlane Syndrome Optic Nerve Hypoplasia, Bilateral Osteochondroma Osteofibrous Dysplasia Overhydrated Hereditary Stomatocytosis Panniculitis Parkinson Disease 15, Autosomal Recessive Early-Onset Periodontal Disease Periodontitis Perrault Syndrome Peters-Plus Syndrome Phace Syndrome Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Adenoma 1, Multiple Types Pituitary Adenoma, Prolactin-Secreting Pituitary Apoplexy Pituitary Gland Disease Pituitary Hormone Deficiency, Combined, 2 Pituitary Hypoplasia Pituitary Stalk Interruption Syndrome Pituitary Tumors Polydactyly Prader-Willi Syndrome Precocious Puberty Primary Agammaglobulinemia Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Pseudohypoparathyroidism, Type Ib Pseudopapilledema Pseudopseudohypoparathyroidism Pycnodysostosis Renal Tubular Acidosis Retinitis Retinitis Pigmentosa Retinoblastoma Rheumatoid Arthritis Rhyns Syndrome Ring Chromosome 18 Robinow Syndrome Rothmund-Thomson Syndrome Rubella Scoliosis Secondary Adrenal Insufficiency Septooptic Dysplasia Short Stature, Idiopathic, X-Linked Shwachman-Diamond Syndrome Silver-Russell Syndrome Sinusitis Situs Inversus Skeletal Dysplasias Skin Disease Sleep Apnea Slipped Capital Femoral Epiphysis Smith-Magenis Syndrome Solitary Median Maxillary Central Incisor Spasticity Spondyloocular Syndrome Stratton-Parker Syndrome Sturge-Weber Syndrome Syringomyelia Temple-Baraitser Syndrome Teratoma Thalassemia Three M Syndrome 1 Thrombosis Thyroiditis Timothy Syndrome Traumatic Brain Injury Trichomegaly with Intellectual Disability, Dwarfism and Pigmentary Degeneration of Retina Trichorhinophalangeal Syndrome Trichorhinophalangeal Syndrome, Type I Trichorhinophalangeal Syndrome, Type Ii Tuberous Sclerosis 1 Tuberous Sclerosis 2 Turner Syndrome Virus-Associated Trichodysplasia Spinulosa Weber Syndrome Williams-Beuren Syndrome Wilson Disease Wolf-Hirschhorn Syndrome