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Nume Dwarfism
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Boli A-Z 12q14 Microdeletion Syndrome Ablepharon-Macrostomia Syndrome Achondrogenesis Achondroplasia Acrofacial Dysostosis, Catania Type Acromegaly Acromesomelic Dysplasia Campailla Martinelli Type Acute Cholinergic Dysautonomia Adrenocortical Carcinoma, Hereditary Agammaglobulinemia Aging Agnosia Alazami Syndrome Al-Gazali-Bakalinova Syndrome Alopecia Alopecia-Contractures-Dwarfism Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amenorrhea Aminoaciduria Ancylostomiasis Aneurysm Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Apparent Mineralocorticoid Excess Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Athetosis Audiogenic Seizures Ayme-Gripp Syndrome Bietti Crystalline Corneoretinal Dystrophy Blepharocheilodontic Syndrome 1 Blepharophimosis Blood Group--Ahonen 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 Boomerang Dysplasia Bowing of Long Bones Congenital Brachydactyly Brittle Bone Disorder Bulimia Nervosa 2 Campomelic Dysplasia Cartilage-Hair Hypoplasia Cartwright Nelson Fryns Syndrome Cataract Cerebral Atrophy Cerebritis Cerebrovascular Disease Cervicitis Cholestasis Chondrodysplasia, Grebe Type Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Choroideremia Ciliopathy Combined Pituitary Hormone Deficiency Conduct Disorder Congenital Hypothyroidism Connective Tissue Disease Constrictive Pericarditis Cornelia De Lange Syndrome Corpus Callosum, Agenesis of, with Abnormal Genitalia Craniosynostosis Crouzon Syndrome with Acanthosis Nigricans Cutis Laxa, Autosomal Recessive, Type Iiia Dermatitis De Sanctis-Cacchione Syndrome Desbuquois Dysplasia 1 Diabetes Insipidus Diabetes Mellitus Diastrophic Dysplasia Dubin-Johnson Syndrome Dubowitz Syndrome Dwarfism, Familial, with Muscle Spasms Dysgammaglobulinemia Dysostosis Dysplastic Cortical Hyperostosis Ectodermal Dysplasia Ellis-Van Creveld Syndrome Encephalocele Ependymoma Epicanthus Epidermoid Cysts Epidermolysis Bullosa Epilepsy Epithelial Recurrent Erosion Dystrophy Exocrine Pancreatic Insufficiency Fabry Disease Familial Osteochondritis Dissecans Fanconi Anemia, Complementation Group E Gastroesophageal Reflux Geleophysic Dwarfism Geleophysic Dysplasia 1 Geleophysic Dysplasia 2 Gigantism Goiter Gonadal Disease Gonadal Dysgenesis Granulocytopenia Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Growth Hormone Deficiency, Isolated Partial Hepatitis Homocystinuria Hydrocephalus Hyper Ige Syndrome Hyperostosis Hyperparathyroidism Hyperpituitarism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Cardiomyopathy Hypochondroplasia Hypoglycemia Hypogonadism Hypophosphatasia Hypophosphatemia Hypopituitarism Hypothalamic Disease Hypothyroidism, Congenital, Nongoitrous, 4 Hypotonia Ichthyosis Ichthyosis Linearis Circumflexa Immunoglobulin E Concentration, Serum Infertility Insulin-Like Growth Factor I Intracranial Aneurysm Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Ia Isolated Growth Hormone Deficiency, Type Ib Isolated Growth Hormone Deficiency, Type Ii Keratosis Keratosis Follicularis, Dwarfism, and Cerebral Atrophy Langer Mesomelic Dysplasia Laron Syndrome Larsen Syndrome Lenz-Majewski Hyperostotic Dwarfism Lethal Short-Limb Skeletal Dysplasia, Al Gazali Type Leukemia Lichen Planus Limb-Girdle Muscular Dystrophy Lipoid Proteinosis of Urbach and Wiethe Lipomatosis Lissencephaly 1 Lissencephaly 4 Lymphoblastic Leukemia Lymphopenia Lysosomal Storage Disease Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Major Affective Disorder 8 Major Affective Disorder 9 Mastoiditis Megalencephaly Meier-Gorlin Syndrome 1 Microcephalic Osteodysplastic Primordial Dwarfism, Type I Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii Microcephalic Primordial Dwarfism, Toriello Type Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microlissencephaly Moebius Syndrome Moyamoya Disease 1 Mucopolysaccharidosis-Plus Syndrome Mulibrey Nanism Muscular Dystrophy Myopia Myxedema Myxopapillary Ependymoma Nephrotic Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuronal Migration Disorders Neuronitis Neutropenia Nievergelt Syndrome Non-Functioning Pituitary Adenoma Oculopalatocerebral Syndrome Omphalocele Onchocerciasis Osteitis Fibrosa Osteochondritis Dissecans Osteochondrodysplasia Osteopoikilosis Pain Agnosia Pancreatitis Paraphilia Disorder Parastremmatic Dwarfism Pericarditis Periodontal Disease Periodontitis Peters-Plus Syndrome Pituitary Gland Disease Pituitary Hypoplasia Polyradiculoneuropathy Porphyria Posterior Polar Cataract Pseudoachondroplasia Pseudopseudohypoparathyroidism Psychosocial Short Stature Ptosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pyle Disease Recessive Dystrophic Epidermolysis Bullosa Renal Dysplasia Retinitis Rickets Robinow Syndrome Rothmund-Thomson Syndrome Schistosomiasis Schneckenbecken Dysplasia Scoliosis Seckel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skeletal Dysplasias Smith-Lemli-Opitz Syndrome Spondylocostal Dysostosis 1, Autosomal Recessive Spondyloepimetaphyseal Dysplasia, Micromelic Spondyloepimetaphyseal Dysplasia, Sponastrime Type Spondyloepiphyseal Dysplasia Congenita Spondyloocular Syndrome Synovial Chondromatosis Taurodontism Telecanthus Terminal Osseous Dysplasia Thanatophoric Dysplasia, Type I Thanatophoric Dysplasia, Type Ii Three M Syndrome 1 Thrombocytopenia Thymic Dysplasia Thyroid Cancer Thyroiditis Tryptophanuria with Dwarfism Turner Syndrome Vohwinkel Syndrome, Variant Form X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome