Informaţii despre

Nume Fanconi Anemia, Complementation Group a
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Constitutional aplastic anaemia
Clasificare anatomică Malacards Boli de piele; Boli de sânge; Boli nefrologice (ale rinichilor); Boli osoase
Boli din aceeaşi familie Fanconi Anemia, Complementation Group I; Fanconi Anemia, Complementation Group J; Fanconi Anemia, Complementation Group L; Fanconi Anemia, Complementation Group N; Fanconi Anemia, Complementation Group O; Fanconi Anemia, Complementation Group P; Fanconi Anemia, Complementation Group Q; Fanconi Anemia, Complementation Group R; Fanconi Anemia, Complementation Group T; Fanconi Anemia, Complementation Group U; Fanconi Anemia, Complementation Group V; Fanconi Anemia, Complementation Group W

Vezi şi

Boli A-Z Acute Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Adenocarcinoma Adenoma Adie Pupil Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alpha-Thalassemia/mental Retardation Syndrome, X-Linked Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Aphthous Stomatitis Aplastic Anemia Artemis Deficiency Arthrochalasia Ehlers-Danlos Syndrome Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Ataxia-Telangiectasia-Like Disorder 1 Baller-Gerold Syndrome Bap1 Tumor Predisposition Syndrome Basal Cell Carcinoma Bednar Tumor Bilateral Breast Cancer Bladder Cancer Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Brca1 Hereditary Breast and Ovarian Cancer Syndrome Breast Cancer Breast-Ovarian Cancer, Familial 1 Breast Reconstruction Cancerophobia Cerebro-Oculo-Facio-Skeletal Syndrome Cervical Cancer Cervicitis Chronic Graft Versus Host Disease Clear Cell Sarcoma Cleft Lip Coats Disease Cockayne Syndrome Colorectal Cancer Congenital Hypoplastic Anemia Congenital Intrauterine Infection-Like Syndrome Corpus Callosum, Agenesis of, with Abnormal Genitalia Crouzon Syndrome with Acanthosis Nigricans Deficiency Anemia Dermatofibrosarcoma Protuberans Diabetes Mellitus Dyskeratosis Congenita Encephalopathy Erythroplakia Familial Thoracic Aortic Aneurysm and Dissection Fanconi Anemia, Complementation Group B Fanconi Anemia, Complementation Group C Fanconi Anemia, Complementation Group D2 Fanconi Anemia, Complementation Group E Fanconi Anemia, Complementation Group F Fanconi Anemia, Complementation Group G Fanconi Anemia, Complementation Group I Fanconi Anemia, Complementation Group J Fanconi Anemia, Complementation Group L Fanconi Anemia, Complementation Group Q Fanconi Syndrome Female Breast Cancer Fetal Alcohol Syndrome Friedreich Ataxia 1 Fundus Albipunctatus Glycerol Kinase Deficiency Graft-Versus-Host Disease Growth Hormone Deficiency Headache Associated with Sexual Activity Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemoglobinuria Hepatic Adenomas, Familial Hepatitis Hepatocellular Adenoma Hepatocellular Carcinoma Hereditary Breast Ovarian Cancer Syndrome Hereditary Site-Specific Ovarian Cancer Syndrome Holoprosencephaly Hydrocephalus Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypoxia Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 Incontinentia Pigmenti Inherited Bone Marrow Failure Syndromes Kagami-Ogata Syndrome Kaufman Oculocerebrofacial Syndrome Laron Syndrome Laryngitis Leukemia Leukoplakia Li-Fraumeni Syndrome Lig4 Syndrome Lobar Holoprosencephaly Lung Cancer Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Lynch Syndrome I Malignant Spiradenoma Maternal Uniparental Disomy of Chromosome 16 Meckel Syndrome, Type 1 Medulloblastoma Melanoma Microphthalmia Microtia-Anotia Miller-Dieker Lissencephaly Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Myelodysplastic Syndrome Myeloid Leukemia Neuroblastoma Nijmegen Breakage Syndrome Nijmegen Breakage Syndrome-Like Disorder Nosophobia Oral Cancer Oral Leukoplakia Oral Squamous Cell Carcinoma Ovarian Cancer Pancreatic Cancer Pancreatitis Pancytopenia Paroxysmal Nocturnal Hemoglobinuria Pharyngitis Polydactyly Polydactyly, Preaxial I Pulmonary Alveolar Proteinosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Roberts Syndrome Sarcoma Scott Syndrome Seckel Syndrome Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Spiradenoma Spondylocarpotarsal Synostosis Syndrome Sporadic Breast Cancer Squamous Cell Carcinoma Stomatitis Synchronous Bilateral Breast Carcinoma Tetraamelia Syndrome, Autosomal Recessive Thyroiditis Torch Syndrome Tracheoesophageal Fistula Tracheoesophageal Fistula with or Without Esophageal Atresia Trichothiodystrophy 1, Photosensitive Uncombable Hair Syndrome 1 Uv-Sensitive Syndrome Vacterl Association Vacterl Association with Hydrocephalus Virus Associated Hemophagocytic Syndrome Vitamin B12 Deficiency Warsaw Breakage Syndrome Werner Syndrome Wilms Tumor 6 Wilson-Turner X-Linked Mental Retardation Syndrome Wiskott-Aldrich Syndrome Xeroderma Pigmentosum, Complementation Group a Xeroderma Pigmentosum, Complementation Group D Xeroderma Pigmentosum, Complementation Group F Xeroderma Pigmentosum, Complementation Group G Xeroderma Pigmentosum, Variant Type Xfe Progeroid Syndrome