Informaţii despre

Nume Ayme-Gripp Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale ochiului; Boli ale urechii; Boli neuronale; Boli psihice

Vezi şi

Boli A-Z 46,xy Sex Reversal 3 Aarskog-Scott Syndrome Adermatoglyphia Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alagille Syndrome 1 Albinism Al-Raqad Syndrome Aminoaciduria Anencephaly Aneurysm Aniridia 1 Anisomastia Ankylosis Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges Anorexia Nervosa 1 Aortic Aneurysm Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Beaulieu-Boycott-Innes Syndrome Blepharophimosis Blood Group--Ahonen 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 Brachydactyly Brachymorphism-Onychodysplasia-Dysphalangism Syndrome Branchiootic Syndrome 1 Bronchomalacia Campomelic Dysplasia Cataract Cayler Cardiofacial Syndrome Chitayat Syndrome Cholestasis Chromosome 16p13.3 Deletion Syndrome, Proximal Chronic Actinic Dermatitis Coloboma of Macula with Type B Brachydactyly Communicating Hydrocephalus Constipation Craniosynostosis 1 Cystic Lymphangioma Dendritic Cell Tumor Dermatitis Diaphragmatic Hernia, Congenital Down Syndrome Dwarfism Dysostosis Ectodermal Dysplasia Ectrodactyly Cardiopathy Dysmorphism Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Periodontal Type, 1 Encephalitis Epilepsy Faciocardiomelic Syndrome Femoral-Facial Syndrome Fibromatosis Fibromatosis, Gingival, with Distinctive Facies Focal Epilepsy Folliculotropic Mycosis Fungoides Fryns Syndrome Gaucher Disease, Type I Gingival Fibromatosis Gingivitis Griscelli Syndrome Growth Control, Y-Chromosome Influenced Hansen's Disease Hepatitis Histiocytosis Hydrocephalus Hypertrichosis Hypoparathyroidism Hypotonia Indeterminate Cell Histiocytosis Jackson-Weiss Syndrome Kbg Syndrome Kozlowski Brown Hardwick Syndrome Kyphomelic Dysplasia Laryngitis Learning Disability Lepromatous Leprosy Limb Reduction Defect Lipomatosis Lissencephaly Lymphangioma Malocclusion and Short Stature Mcdonough Syndrome Mesomelia Microcephaly Multicentric Reticulohistiocytosis Multiple Epiphyseal Dysplasia Mutism Mycosis Fungoides Myopathy Nephrotic Syndrome Neuronitis Night Blindness Oculocutaneous Albinism Oligohydramnios Omphalocele Osteomalacia Papillon-Lefevre Syndrome Periodontitis Pharyngitis Pierpont Syndrome Polydactyly Polyvalvular Heart Disease Syndrome Potocki-Lupski Syndrome Primary Lateral Sclerosis, Adult, 1 Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Rheumatoid Arthritis Ring Chromosome 18 Robinow Syndrome, Autosomal Recessive Scott Syndrome Seizure Disorder Sensorineural Hearing Loss Solitary Median Maxillary Central Incisor Speech Disorder Spondyloenchondrodysplasia Supravalvular Aortic Stenosis Systemic Mastocytosis Tetralogy of Fallot Three M Syndrome 1 Thrombocytopenia Thrombocytopenia Robin Sequence Ulnar-Mammary Syndrome Ventricular Septal Defect Williams-Beuren Syndrome