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Nume Hypogonadotropic Hypogonadism
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hypopituitarism; Klinefelter syndrome karyotype 47,XXY; Klinefelter syndrome, unspecified
Clasificare anatomică Malacards Boli endocrine

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Boli A-Z 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy 47, Xxy 48,xxyy Syndrome 49,xxxxy Syndrome Acanthosis Nigricans Acute Leukemia Acute Monoblastic Leukemia Adenocarcinoma Adenoma Adrenal Carcinoma Adrenal Hypoplasia, Congenital Agammaglobulinemia Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amenorrhea Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorchia Anorexia Nervosa 1 Anosmia Anovulation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Autoimmune Disease Autoimmune Hepatitis Azoospermia Bilateral Breast Cancer Biotin Deficiency Bipolar Disorder Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock 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 Brain Germinoma Breast Cancer Capillary Hemangioma Cataract Cat Eye Syndrome Central Nervous System Germinoma Central Nervous System Lymphoma Central Precocious Puberty Cerebellar Degeneration Cerebellar Hypoplasia Cerebritis Charge Syndrome Chiari Malformation Cholelithiasis Choriocarcinoma Chorioretinitis Choroiditis Chromosomal Triplication Chromosome 17q Duplication Chromosome 9 Inversion Chronic Pain Chronic Ulcer of Skin Cleidocranial Dysplasia Spectrum Disorder Combined Pituitary Hormone Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Hypothyroidism Congenital Toxoplasmosis Conjunctivitis Connective Tissue Disease Craniopharyngioma Cryptorchidism, Unilateral or Bilateral Cystic Fibrosis Cytomegalic Congenital Adrenal Hypoplasia Diabetes Insipidus Diabetes Mellitus Dyskeratosis Congenita, X-Linked Dysostosis Dystrophinopathies Ectopic Pregnancy Embryonal Carcinoma Empty Sella Syndrome Endocarditis Endotheliitis Ependymoma Epidermoid Cysts Essential Tremor Eunuchism Extragonadal Germ Cell Cancer Fatty Liver Disease Floating-Harbor Syndrome Germ Cells Tumors Giant Cell Myocarditis Glycogen Storage Disease Gonadal Disease Gonadal Dysgenesis Gorlin-Chaudhry-Moss Syndrome Graves' Disease Growth Hormone Deficiency Gynecomastia Hartsfield Syndrome Headache Hemangioma Hemochromatosis, Type 1 Hepatitis Hereditary Hemorrhagic Telangiectasia Hermaphroditism Histiocytosis Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperostosis Hyperostosis Frontalis Interna Hyperparathyroidism Hyperprolactinemia Hypoadrenocorticism, Familial Hypogonadism Hypogonadism, Male Hypogonadotropic Hypogonadism 23 Without Anosmia Hypogonadotropic Hypogonadism 7 with or Without Anosmia Hypogonadotropism Hypomyelinating Leukodystrophy Hypoparathyroidism Hypopituitarism Hypospadias Hypothalamic Hamartomas Hypotrichosis 1 Ichthyosis Idiopathic Central Precocious Puberty Idiopathic Hemiconvulsion-Hemiplegia Syndrome Incontinentia Pigmenti Infant Gynecomastia Infertility Isolated Gonadotropin-Releasing Hormone Deficiency Kallmann Syndrome Kindler Syndrome Kniest Dysplasia Laugier-Hunziker Syndrome Leukemia Leukodystrophy Leydig Cell Tumor Liver Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphoblastic Leukemia Lymphoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macs Syndrome Major Affective Disorder 8 Major Affective Disorder 9 Male Infertility Malignant Histiocytosis Malignant Leydig Cell Tumor Malignant Teratoma Mature Teratoma Mccune-Albright Syndrome Mediastinitis Megalencephaly Microcephaly Microphthalmia Mixed Connective Tissue Disease Moebius Syndrome Muscular Atrophy Muscular Dystrophy Myasthenia Gravis Myelodysplastic Syndrome Myeloid Leukemia Myopathy Myotonia Myotonia Atrophica Neuronitis Neutropenia Normosmic Congenital Hypogonadotropic Hypogonadism Ovarian Disease Paranoid Schizophrenia Partial Deletion of Y Penis Agenesis Penoscrotal Transposition Persistent Mullerian Duct Syndrome Pituitary Hormone Deficiency, Combined, 2 Poland Syndrome Polymyositis Prader-Willi Syndrome Precocious Puberty Premature Ejaculation Premature Ovarian Failure 1 Primary Central Nervous System Lymphoma Primary Hyperparathyroidism Progressive Muscular Atrophy Prostatitis Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Pseudovaginal Perineoscrotal Hypospadias Psoriasis Psoriasis 13 Psychotic Disorder Pulmonary Alveolar Microlithiasis Pulmonary Embolism Pyoderma Pyoderma Gangrenosum Rapp-Hodgkin Syndrome Renal Tubular Acidosis Retinitis Pigmentosa 67 Rheumatic Disease Rheumatoid Arthritis Rickets Schizophrenia Seminoma Sensorineural Hearing Loss Spastic Ataxia, Charlevoix-Saguenay Type Spermatogenic Failure, X-Linked, 1 Spinal Cord Injury Split Hand Split Hand-Foot Malformation Spondylitis Spondyloarthropathy 1 Squamous Cell Carcinoma Synostoses, Tarsal, Carpal, and Digital Synostosis Systemic Lupus Erythematosus Taurodontism Teratoma Testicular Microlithiasis Thalassemia Thrombosis Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxoplasmoză Transposition of the Great Arteries Transsexualism Transsexuality Transvestism Tremor Triple X Syndrome Tumoral Calcinosis, Hyperphosphatemic, Familial Undifferentiated Pleomorphic Sarcoma Van Maldergem Syndrome Varicocele Vasculitis Venous Insufficiency Ventricular Fibrillation, Paroxysmal Familial, 1 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 West Syndrome Wolff-Parkinson-White Syndrome Woodhouse-Sakati Syndrome