Informaţii despre

Nume Polycystic Ovary Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Polycystic ovarian syndrome
Clasificare anatomică Malacards Boli endocrine
Boli din aceeaşi familie Polycystic Ovary Syndrome 1

Vezi şi

Boli A-Z 3-Beta-Hydroxysteroid Dehydrogenase Deficiency 46 Xy Gonadal Dysgenesis Abdominal Obesity-Metabolic Syndrome 1 Acanthosis Nigricans Acquired Metabolic Disease Acrocallosal Syndrome Acromegaly Acute Adrenal Insufficiency Acute Insulin Response Adenocarcinoma Adenoma Adrenal Adenoma Adrenal Carcinoma Adrenal Cortical Adenoma Adrenal Gland Hyperfunction Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenal Rest Tumor Adrenocortical Carcinoma, Hereditary Aging Alopecia Alopecia, Androgenetic, 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Anauxetic Dysplasia 1 Androgenic Alopecia Androgen Insensitivity, Partial Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Angioedema Aniridia 1 Anorexia Nervosa 1 Anovulation Anterior Cutaneous Nerve Entrapment Syndrome Antley-Bixler Syndrome Aromatase Deficiency Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atherosclerosis Susceptibility Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Autonomic Dysfunction Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 1 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 Borderline Personality Disorder Breast Disease Bulimia Nervosa 2 Central Precocious Puberty Cervicitis Cherubism Chlamydia Chromophobe Adenoma Chromosomal Triplication Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conjunctivitis Corticosteroid-Binding Globulin Deficiency Cortisone Reductase Deficiency Craniopharyngioma Cryptorchidism, Unilateral or Bilateral Cystadenoma Cytochrome P450 Oxidoreductase Deficiency Diabetes Mellitus Donohue Syndrome Eating Disorder Eclampsia Ectopic Pregnancy Empty Sella Syndrome Endocrine Pancreas Disease Endometrial Adenocarcinoma Endometrial Cancer Endometrial Disease Endometriosis of Uterus Endotheliitis Estrogen Excess Familial Partial Lipodystrophy Fanconi Anemia, Complementation Group E Fatty Liver Disease Female Reproductive System Disease Fetal Macrosomia Galactorrhea Generalized Anxiety Disorder Gestational Diabetes Gingivitis Glucose Intolerance Glucose Metabolism Disease Goiter Gonadal Disease Graves' Disease Gynecomastia Headache Helicobacter Pylori Infection Hepatic Adenomas, Familial Hepatitis Hepatocellular Adenoma Hereditary Angioedema Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Homocysteinemia Hyperandrogenism Hyperandrogenism Due to Cortisone Reductase Deficiency Hyperglycemia Hyperinsulinism Hyperpituitarism Hyperproinsulinemia Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoactive Sexual Desire Disorder Hypoadrenocorticism, Familial Hypoalphalipoproteinemia, Primary Hypoglycemia Hypogonadotropism Hypopituitarism Idiopathic Central Precocious Puberty Immunodeficiency 23 Impotence Infertility Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Intracranial Hypertension Laugier-Hunziker Syndrome Leiomyoma, Uterine Leydig Cell Tumor Lipid Metabolism Disorder Lipodystrophy Lipodystrophy, Familial Partial, Type 2 Lipoid Congenital Adrenal Hyperplasia Lissencephaly 1 Liver Disease Luteoma Lutheran Suppressor, X-Linked Lymphocytic Hypophysitis Malignant Hyperthermia 1 Malignant Spiradenoma Mammographic Density Mccune-Albright Syndrome Meckel Syndrome, Type 1 Microglandular Adenosis Migraine with or Without Aura 1 Mitochondrial Disorders Mixed Cell Adenoma Miyoshi Muscular Dystrophy 1 Mood Disorder Morbid Obesity Mosaic Variegated Aneuploidy Syndrome Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Myelodysplastic Syndrome Myoma Neurofibromatosis, Type Ii Nodular Goiter Nonalcoholic Steatohepatitis Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Nutritional Deficiency Disease Occipital Horn Syndrome Oocyte Maturation Defect 1 Ovarian Disease Ovarian Hyperstimulation Syndrome Overhydrated Hereditary Stomatocytosis Pancreatitis Papilledema Penis Agenesis Personality Disorder Peutz-Jeghers Syndrome Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Apoplexy Pituitary-Dependent Cushing's Disease Pituitary Gland Disease Pituitary Infarct Polycystic Ovary Syndrome 1 Prader-Willi Syndrome Precocious Puberty Precocious Puberty, Male-Limited Prediabetes Syndrome Pre-Eclampsia Premature Ovarian Failure 1 Premenstrual Tension Prostatic Adenoma Prostatitis Pseudohermaphroditism Pseudohypoparathyroidism, Type Ia Psoriasis Psoriasis 13 Pustulosis Palmaris Et Plantaris Refractory Anemia Reproductive System Disease Retinitis Salivary Gland Adenoma, Pleomorphic Secondary Adrenal Insufficiency Sex Differentiation Disease Sheehan Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sleep Apnea Spastic Ataxia, Charlevoix-Saguenay Type Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Steroid Inherited Metabolic Disorder Teratoma Testicular Leydig Cell Tumor Tetraploidy Thrombocytosis Thrombophilia Thrombosis Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Transsexualism Transsexuality Trisomy 12 Mosaicism Turner Syndrome Ulna and Fibula, Absence of, with Severe Limb Deficiency Vaginitis Varicocele Vascular Disease Ventricular Fibrillation, Paroxysmal Familial, 1 Vogt-Koyanagi-Harada Disease Wilms Tumor 1 Wilms Tumor 6