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Differential Diagnosis For Hemoglobin (Lab) - Decreased: Hereditary, Familial, Genetic Disorders
- Trauma Causes (3)
- Electromagnetic, Physics, trauma, Radiation Causes (2)
- Iatrogenic, Self Induced Disorders (3)
- Surgical, Procedure Complication (5)
- Infectious Disorders (Specific Agent) (58)
- Infected organ, Abscesses (9)
- Granulomatous, Inflammatory Disorders (3)
- Neoplastic Disorders (58)
- Allergic, Collagen, Auto-Immune Disorders (39)
- Metabolic, Storage Disorders (14)
- Biochemical Disorders (1)
- Deficiency Disorders (22)
- Congenital, Developmental Disorders (6)
- Hereditary, Familial, Genetic Disorders (24)
- Usage, Degenerative, Necrosis, Age Related Disorders (1)
- Relational, Mental, Psychiatric Disorders (1)
- Anatomic, Foreign Body, Structural Disorders (17)
- Functional, Physiologic Variant Disorders (5)
- Vegetative, Autonomic, Endocrine Disorders (14)
- Reference to Organ System (49)
- Pathophysiologic (7)
- Heirarchical Major Groups (2)
- Drugs (6)
- Poisoning (Specific Agent) (8)
- Organ Poisoning (Intoxication) (2)
- Synonyms (10)
- Definition
- External Links Related to Hemoglobin (Lab) - Decreased
- Hereditary, Familial, Genetic Disorders:
Sickle cell crisis
Hemoglobin E thalassemia
Hemoglobinopathy
Telangiectasia,hereditary hemorrhagic
Granulomatous dis/childhood, chronic
Sickle cell/thalassemia disease
Thalassemia major
Thalassemia minor
Spherocytosis, crisis phase
Heinz body hereditary anemia
Hereditary hemolytic anemia syndromes
Hereditary sideroblastic anemia
Pyruvate kinase deficiency RBC's
Sickle cell anemia
Spherocytosis, hereditary
Hemoglobin H disease
Cystic fibrosis (mucoviscidosis)
Elliptocytosis, hereditary
Hemoglobin C disease
Polycystic kidney disease
Anemia, hereditary hemolytic,nonspher'c
Fanconi's pancytopenia-dysmelia synd
Thalassemia-hemoglobin C disease
Lepore Hemoglobinopathy