Inheritance gene autosomal recessive anemia hemolytic. Medical search. Frequent questions

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Anatomy19

Erythrocytes Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 1 X Chromosome Heinz Bodies Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 16 Erythrocytes, Abnormal Chromosomes, Human, Pair 5 Erythrocyte Membrane Chromosomes, Human, Pair 6 Fundus Oculi Chromosomes, Human, Pair 7 Fibroblasts Cell Line Chromosomes, Human, Pair 9 Kidney Chromosomes, Human, Pair 11 Cells, Cultured

Organisms4

Infectious Anemia Virus, Equine Chicken anemia virus Mice, Mutant Strains Mice, Inbred C57BL

Diseases105

Anemia Anemia, Hemolytic Anemia, Hemolytic, Autoimmune Anemia, Hemolytic, Congenital Hemolysis Anemia, Aplastic Fanconi Anemia Polycystic Kidney, Autosomal Recessive Syndrome Anemia, Hemolytic, Congenital Nonspherocytic Hemolytic-Uremic Syndrome Anemia, Hypochromic Abnormalities, Multiple Retinitis Pigmentosa Anemia, Macrocytic Anemia, Pernicious Anemia, Sickle Cell Microcephaly Anemia, Megaloblastic Anemia, Sideroblastic Ichthyosis Hypotrichosis Intellectual Disability Ichthyosiform Erythroderma, Congenital Dwarfism Anemia, Refractory Deafness Osteochondrodysplasias Genetic Diseases, Inborn Hearing Loss, Sensorineural Anemia, Dyserythropoietic, Congenital Muscular Dystrophies Ichthyosis, Lamellar Cerebellar Ataxia Chromosome Disorders Bone Diseases, Developmental Nails, Malformed Genetic Predisposition to Disease Metabolism, Inborn Errors Spherocytosis, Hereditary Equine Infectious Anemia Eye Diseases, Hereditary Osteopetrosis Erythroblastosis, Fetal Foot Deformities, Congenital Charcot-Marie-Tooth Disease Ectodermal Dysplasia Hand Deformities, Congenital Anemia, Diamond-Blackfan Syndactyly Albinism, Oculocutaneous Dysostoses Optic Atrophy Hearing Loss Microphthalmos Cutis Laxa Eye Abnormalities Disease Models, Animal Muscle Hypotonia Pregnancy Complications, Hematologic Muscular Atrophy, Spinal Amino Acid Metabolism, Inborn Errors Retinal Degeneration Friedreich Ataxia Kidney Diseases, Cystic Polycystic Kidney Diseases Spastic Paraplegia, Hereditary Hair Diseases Dog Diseases Cystinosis Keratoderma, Palmoplantar Bardet-Biedl Syndrome Facies Granulomatous Disease, Chronic Genetic Diseases, X-Linked Arthrogryposis Tooth Abnormalities Anemia, Neonatal Ectromelia Myotonia Congenita Craniofacial Abnormalities Spinal Muscular Atrophies of Childhood Glucosephosphate Dehydrogenase Deficiency Anemia, Refractory, with Excess of Blasts Hereditary Sensory and Autonomic Neuropathies Acidosis, Renal Tubular Polydactyly Night Blindness Cataract Muscular Diseases Chromosome Aberrations Immunologic Deficiency Syndromes Ataxia Telangiectasia Limb Deformities, Congenital Familial Mediterranean Fever Epidermolysis Bullosa Ataxia Caroli Disease Porphyria, Erythropoietic Spinocerebellar Degenerations Lipoid Proteinosis of Urbach and Wiethe Usher Syndromes Thrombocytopenia Alopecia Nephritis, Hereditary

Chemicals and Drugs34

Hemolytic Agents Hemolysin Proteins Codon, Nonsense Hemoglobins Genetic Markers Fanconi Anemia Complementation Group Proteins Iron Erythropoietin Membrane Proteins Fanconi Anemia Complementation Group A Protein Phenylhydrazines Fanconi Anemia Complementation Group C Protein Eye Proteins DNA Primers DNA Sarcoglycans Fanconi Anemia Complementation Group D2 Protein Survival of Motor Neuron 1 Protein DNA, Mitochondrial Fanconi Anemia Complementation Group G Protein Proteins Hematinics RNA Splice Sites Rh-Hr Blood-Group System Complement System Proteins SMN Complex Proteins Ubiquitin-Protein Ligases Streptolysins Ferritins RNA, Messenger Recombinant Proteins Nerve Tissue Proteins Hemoglobins, Abnormal Carrier Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment33

Pedigree DNA Mutational Analysis Chromosome Mapping Crosses, Genetic Coombs Test Heterozygote Detection Models, Genetic Polymerase Chain Reaction Genetic Testing Sequence Analysis, DNA Complement Hemolytic Activity Assay Hemolytic Plaque Technique Erythrocyte Count Electroretinography Disease Models, Animal Reticulocyte Count Hematocrit Facies Osmotic Fragility Fatal Outcome Blood Transfusion Amino Acid Substitution Genetic Complementation Test Erythrocyte Indices Sequence Alignment Cloning, Molecular Prenatal Diagnosis Hemoglobinometry Hybridization, Genetic Pigmentation Genetic Association Studies Case-Control Studies Physical Chromosome Mapping

Psychiatry and Psychology4

Intellectual Disability Family Siblings Nuclear Family

Phenomena and Processes67

Genes, Recessive Consanguinity Inheritance Patterns Hemolysis Mutation Homozygote Genetic Linkage Phenotype Genes, Dominant Heterozygote Lod Score Mutation, Missense Alleles Base Sequence Genotype Exons Codon, Nonsense Haplotypes Heredity Genetic Markers Amino Acid Sequence Frameshift Mutation Genetic Heterogeneity Extrachromosomal Inheritance Microsatellite Repeats Point Mutation Founder Effect Multifactorial Inheritance Exome Genetic Predisposition to Disease Chromosomes, Human, Pair 2 Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Chromosomes, Human, Pair 1 X Chromosome Gene Frequency Erythrocyte Count Sequence Deletion Genetic Variation Penetrance Polymorphism, Single Nucleotide Reticulocyte Count Hematocrit Gene Deletion Pregnancy Chromosomes, Human, Pair 19 Genes, Lethal Chromosomes, Human, Pair 16 Erythrocyte Aging Osmotic Fragility Erythropoiesis Introns Chromosomes, Human, Pair 5 Polymorphism, Restriction Fragment Length Amino Acid Substitution Chromosomes, Human, Pair 6 Erythrocyte Indices Chromosome Aberrations RNA Splice Sites Sequence Homology, Amino Acid Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 11 Hybridization, Genetic Pigmentation Recombination, Genetic Genetic Loci

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena3

Family Siblings Nuclear Family

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Fatal Outcome

Named Groups4

Infant, Newborn Arabs Jews Siblings

Health Care6

Family Health Genetic Testing Age of Onset Fatal Outcome Genetic Counseling Case-Control Studies

Geographicals5

Pakistan Tunisia Israel Lebanon Morocco

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Genes, Recessive Anemia Anemia, Hemolytic Anemia, Hemolytic, Autoimmune Consanguinity Pedigree Inheritance Patterns Anemia, Hemolytic, Congenital Hemolysis Mutation Anemia, Aplastic Hemolytic Agents Homozygote Fanconi Anemia Polycystic Kidney, Autosomal Recessive Syndrome Genetic Linkage Phenotype DNA Mutational Analysis Anemia, Hemolytic, Congenital Nonspherocytic Chromosome Mapping Genes, Dominant Hemolytic-Uremic Syndrome Heterozygote Lod Score Anemia, Hypochromic Abnormalities, Multiple Mutation, Missense Molecular Sequence Data Retinitis Pigmentosa Anemia, Macrocytic Anemia, Pernicious Anemia, Sickle Cell Microcephaly Alleles Base Sequence Genotype Anemia, Megaloblastic Crosses, Genetic Anemia, Sideroblastic Erythrocytes Hemolysin Proteins Exons Codon, Nonsense Ichthyosis Haplotypes Hypotrichosis Hemoglobins Coombs Test Heredity Genetic Markers Amino Acid Sequence Frameshift Mutation Intellectual Disability Family Health Infectious Anemia Virus, Equine Genetic Heterogeneity Ichthyosiform Erythroderma, Congenital Heterozygote Detection Dwarfism Anemia, Refractory Deafness Extrachromosomal Inheritance Microsatellite Repeats Models, Genetic Pakistan Osteochondrodysplasias Infant, Newborn Genetic Diseases, Inborn Hearing Loss, Sensorineural Anemia, Dyserythropoietic, Congenital Fanconi Anemia Complementation Group Proteins Point Mutation Founder Effect Muscular Dystrophies Polymerase Chain Reaction Ichthyosis, Lamellar Multifactorial Inheritance Cerebellar Ataxia Chromosome Disorders Bone Diseases, Developmental Genetic Testing Exome Nails, Malformed Genetic Predisposition to Disease Sequence Analysis, DNA Age of Onset Iron Chromosomes, Human, Pair 2 Polymorphism, Single-Stranded Conformational Metabolism, Inborn Errors Complement Hemolytic Activity Assay Erythropoietin Spherocytosis, Hereditary Hemolytic Plaque Technique Equine Infectious Anemia Arabs Eye Diseases, Hereditary Polymorphism, Genetic Osteopetrosis

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