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Nume Lipoid Congenital Adrenal Hyperplasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Adrenogenital disorder, unspecified; Congenital adrenogenital disorders associated with enzyme deficiency
Clasificare anatomică Malacards Boli ale sistemului reproducator; Boli endocrine

Vezi şi

Boli A-Z 3-Beta-Hydroxysteroid Dehydrogenase Deficiency 46,xx Sex Reversal 1 46 Xy Gonadal Dysgenesis 46,xy Sex Reversal 3 Acanthosis Nigricans Achalasia-Addisonianism-Alacrima Syndrome Acute Adrenal Insufficiency Adenocarcinoma Adenoma Adrenal Adenoma Adrenal Carcinoma Adrenal Cortex Disease Adrenal Cortical Adenoma Adrenal Cortical Hypofunction Adrenal Gland Disease Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency Adrenal Hypoplasia, Congenital Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenal Rest Tumor Adrenocortical Carcinoma, Hereditary Aggressive Periodontitis Aging Aldosterone-Producing Adenoma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Amenorrhea Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorchia Anorexia Nervosa 1 Antley-Bixler Syndrome Apparent Mineralocorticoid Excess Aromatase Deficiency Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Autosomal Recessive Disease Azoospermia Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 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 Bruxism Central Precocious Puberty Cholestasis Chromosome 6p Deletion Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Cleft Larynx, Posterior Complete Androgen Insensitivity Syndrome Congenital Hypothyroidism Congestive Heart Failure Conn's Syndrome Cortical Blindness Cystadenoma Cystic Fibrosis Cytochrome P450 Oxidoreductase Deficiency Diabetes Mellitus Diaphanospondylodysostosis Diarrhea Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency Ehlers-Danlos Syndrome Encephalopathy Endocrine Organ Benign Neoplasm Epilepsy Familial Glucocorticoid Deficiency Fanconi Anemia, Complementation Group E Galactosialidosis Glucocorticoid Deficiency 1 Glucocorticoid-Induced Osteoporosis Gonadal Disease Growth Hormone Deficiency Helix Syndrome Hemiplegia Hepatic Adenomas, Familial Hepatitis Hyperaldosteronism, Familial, Type I Hyperandrogenism Hyperprolactinemia Hypertelorism, Microtia, Facial Clefting Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoadrenocorticism, Familial Hypoaldosteronism Hypoglycemia Hypogonadotropism Hypokalemia Hypospadias Hypothalamic Hamartomas Idiopathic Hemiconvulsion-Hemiplegia Syndrome Inappropriate Adh Syndrome Infertility Inherited Metabolic Disorder Insulin-Like Growth Factor I Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Keratoconus Leydig Cell Tumor Luteoma Male Infertility Malignant Hypertension Malignant Leydig Cell Tumor Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency Meningioma, Familial Mucinous Ovarian Cystadenoma Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis Type Vi Muscular Dystrophy Myotonia Congenita, Autosomal Dominant Nephrocalcinosis Neuraminidase Deficiency Neuroblastoma Neurofibromatosis, Type Ii Nicolaides-Baraitser Syndrome Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Normokalemic Periodic Paralysis Occipital Horn Syndrome Organ System Benign Neoplasm Orofacial Cleft Ovarian Cyst Ovarian Cystadenoma Ovarian Disease Overhydrated Hereditary Stomatocytosis Periodontitis Phenylketonuria Polycystic Ovary Syndrome Porphyria Porphyria Cutanea Tarda Postural Hypotension Prader-Willi Syndrome Precocious Puberty Premature Ovarian Failure 7 Prostatitis Pseudohermaphroditism Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudohypoaldosteronism Pyloric Stenosis Renal Hypertension Saethre-Chotzen Syndrome Salivary Gland Adenoma, Pleomorphic Sex Differentiation Disease Sleep Apnea Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Steroid Inherited Metabolic Disorder Supernumerary Nostril Suprasellar Meningioma Sveinsson Chorioretinal Atrophy Testicular Leydig Cell Tumor Testicular Microlithiasis Thalassemia Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Transient Pseudohypoaldosteronism Transsexualism Triple X Syndrome Turner Syndrome Vaginitis Waterhouse-Friderichsen Syndrome