Informaţii despre

Nume Cutis Laxa
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Other specified congenital malformations of skin
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare; Boli de piele; Boli gastrointestinale; Boli nefrologice (ale rinichilor); Boli neuronale; Boli osoase; Boli psihice
Boli din aceeaşi familie Acquired Cutis Laxa; Cutis Laxa, Autosomal Dominant 1; Cutis Laxa, Autosomal Dominant 2; Cutis Laxa, Autosomal Dominant 3; Cutis Laxa, Autosomal Recessive Type 1; Cutis Laxa, Autosomal Recessive, Type Ia; Cutis Laxa, Autosomal Recessive, Type Ib; Cutis Laxa, Autosomal Recessive, Type Ic; Cutis Laxa, Autosomal Recessive, Type Iia; Cutis Laxa, Autosomal Recessive, Type Iib; Cutis Laxa, Autosomal Recessive, Type Iic; Cutis Laxa, Autosomal Recessive, Type Iid; Cutis Laxa, Autosomal Recessive, Type Iiia; Cutis Laxa, Autosomal Recessive, Type Iiib

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Boli A-Z Ablepharon-Macrostomia Syndrome Acquired Cutis Laxa Aging Alopecia Al-Raqad Syndrome Amyloidosis Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortitis Apolipoprotein C-Iii Deficiency Arterial Tortuosity Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Atp6v0a2-Related Cutis Laxa Autosomal Recessive Cutis Laxa Type 2, Classic Type Baroreflex Failure Bleeding Disorder, Platelet-Type, 11 Blepharochalasis Blood Group--Ahonen Blood Group, I System Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brittle Bone Disorder Cataract Celiac Disease 1 Cerebritis Chromosome 11p Duplication Conjunctivochalasis Connective Tissue Disease Costello Syndrome Craniosynostosis 1 Cutaneous Mastocytosis Cutis Laxa, Autosomal Dominant 1 Cutis Laxa, Autosomal Recessive Type 1 Cutis Laxa, Autosomal Recessive, Type Ia Cutis Laxa, Autosomal Recessive, Type Ic Cutis Laxa, Autosomal Recessive, Type Iia Cutis Laxa, Autosomal Recessive, Type Iib Cutis Laxa, Autosomal Recessive, Type Iiia Dandy-Walker Syndrome De Barsy Syndrome Dermatitis Dermatitis Herpetiformis Ectropion Efemp2-Related Cutis Laxa Ehlers-Danlos Syndrome Elastoderma Elastosis Perforans Serpiginosa Entropion Epilepsy Exocrine Pancreatic Insufficiency Fanconi Anemia, Complementation Group E Fbln5-Related Cutis Laxa Geroderma Osteodysplasticum Granulomatous Dermatitis Heavy Chain Deposition Disease Hernia, Hiatus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Pyloric Stenosis Hypothyroidism, Congenital, Nongoitrous, 4 Ichthyosis Inguinal Hernia Intussusception Kabuki Syndrome 1 Keutel Syndrome Lacrimal Duct Defect Leukodystrophy Light and Heavy Chain Deposition Disease Lipoid Proteinosis of Urbach and Wiethe Ltbp4-Related Cutis Laxa Lung Disease Lupus Erythematosus Lymphoma Macrostomia, Isolated Macs Syndrome Marden-Walker Syndrome Marshall Syndrome Mast Cell Activation Syndrome Menkes Disease Microcephaly Mid-Dermal Elastolysis Mucopolysaccharidosis, Type Vii Mycosis Fungoides Myeloma, Multiple Myopathy Myopia Nephrotic Syndrome Occipital Horn Syndrome Oligohydramnios Optic Disk Drusen Osseous Heteroplasia, Progressive Pachygyria Pancreatitis Patterson Pseudoleprechaunism Syndrome Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis Plasmacytoma Pneumonia Polymicrogyria Pseudoxanthoma Elasticum Pulmonary Emphysema Pulmonary Hypertension Purpura Pyloric Stenosis Renal Hypodysplasia/aplasia 1 Renal Tubular Acidosis Retinitis Retinitis Pigmentosa Rheumatoid Arthritis Sarcoidosis 2 Scarf Syndrome Scleromyxedema Scoliosis Sengers Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skeletal Dysplasias Skin Disease Sotos Syndrome 1 Supravalvular Aortic Stenosis Systemic Lupus Erythematosus Tetraamelia Syndrome, Autosomal Recessive Thyroiditis Urticaria Vasculitis Warburg Micro Syndrome Weber Syndrome Wrinkles Wrinkly Skin Syndrome