- Differential Diagnosis
- Diseases
- Drugs
- More
-
- Try building your search one term at a time, and be as specific as you can! Search term example: "chronic cough".
- Do not enter multiple findings such as "anemia, chronic cough, weight loss, vomiting" all at the same time.
- After selecting your term from the search results a list of possible diagnoses will be generated. If the list is too long, you will be able to narrow it down by entering additional terms.
- Do not enter values such as "heart rhythm 110" or "sodium 125", instead use "tachycardia" or "hyponatremia".
- Disease Information
- Disease Comparison
-
Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
- Eponymic
- Functional-Physiologic
- Hereditofamilial
- Iatrogenic
- Idiopathic
- Infected Organ-Abcess
- Infectious agent
- Inflammatory-Granulomatous
- Metabolic-Storage
- Neoplastic
- Poison Agent
- Poisoned Organ
- Radiation-Xray-trauma
- Mental
- Structural-Anatomic-Foreign body
- Surgical Procedure-Complication
- Trauma
- Use-age-Atrophic
- Endocrine-Vegetative
-
Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Comparison Results (show all mode) for Hemophilia and Myopathy, Myotubular/Centronuclear
Myopathy, Myotubular/Centronuclear
Found: 65 | Differences: 60
Found: 163 | Differences: 158
Hemophilia and Myopathy, Myotubular/Centronuclear sharing 5 common findings. (show all, show common, show differences)
- Clinical Manifestations
- Signs & Symptoms
- Hyperextensable Joints Infant
- Constipation Children
- Tongue Protrudes Infant
- Calf enlargement/bilateral
- Delay Sitting Unsupported Infant
- Hypotonia
- Mouth Hangs Open Infant
- Muscle weakness
- Muscles Soft/Doughy Infant
- Proximal muscle weakness
- Rolling Over Delay Infant
- Babkin infant sign/Abnormal
- Delayed walking milestone/child
- Development Motor Skills (Milestones) Delayed
- Facial muscle weakness/myopathy
- Galant Infant reflex/Abnormal
- Head Neck Floppy Infant Hypotonia Sign
- Hyporeflexia/DTRs decreased
- Infant Head Support Delay
- Moro reflex Poor/Absent Infant
- Palmar Grasp infant Reflex Abnormal
- Primitive infant reflexes/Abnormal
- Rooting infant sign/Abnormal
- Swimming infant reflex/Abnormal
- Tonic Neck Infant reflex/Abnormal
- Shallow Breathing Infant
- Snoring
- Weakness
- Double Image Vision Confirmed
- Ptosis (blepharoptosis)
- Demographics & Risk Factors
- Population Group
- Infant
- Family History
- Family history/Muscle disease/Muscular dystrophy
- Sex & Age Groups
- Population/Infant
- Population/Infant male
- Population/Male
- Diagnostic Test Results
- Pathology
- BX/Muscle biopsy/centralization of nuclei
- Electrodiagnosis
- EMG/Abnormal findings
- EMG/Myotonic muscle activity
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Eaton-Lambert syndrome
- Muscular dystrophy
- Polymyositis
- Respiratory muscle weakness
- Associated Disease & Complications - Causes
- Acute respiratory failure/Respiratory arrest
- Apnea
- Metabolic Myopathy
- Myopathy
- Neonatal Hypotonia/Floppy Baby Syndrome
- Ophthalmoplegia
- Ophthalmoplegia/progressive/ext/chronic
- Respiratory neonatal distress syndrome
- Disease Mechanism & Classification
- Class
- CLASS/Muscle disorder (ex)
- CLASS/Striated muscle disorder (ex)
- Pathophysiology
- Pathophysiology/Gene locus Chromosome X.
- Pathophysiology/Maternal Chromosome mutation
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Autosomal recessive disorder (ex)
- PROCESS/Disease with many subtypes (ex)
- PROCESS/Genetic disorder/Spontaneous mutations/sporadic
- PROCESS/Hereditofamilial (category)
- PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
- Clinical Manifestations
- Signs & Symptoms
- Bleeding from venipuncture sites/needle stick
- Bleeding/excessive from mild trauma
- Bruising/Ecchymosis
- Purpura
- Excessive/easy bruising tendency
- Bruises/abdomen
- Rectal bleeding, gross red
- Rectal Blood/Bleeding
- Bleeding from Mouth in Elderly
- Bleeding from mouth/oral blood
- Bleeding gums
- Bleeding/prolonged dental surgery
- Blood in mouth/gums/throat
- Hip Inner Thigh Pain
- Vaginal Bleeding
- Vaginal bleeding/child
- Hemoptysis
- Arthralgias Polyarthralgias
- Asymmetric hand/feet arthritis
- Bilateral knee pains
- Discolored Bruised Joint
- Discolored Bruised Knee
- Enlarged/deformed joints
- Hip Pain
- Hip Pain In a Child
- Hot Joint
- Intermittant arthritis syndrome
- Joint deformities
- Joint effusion
- Joint Pains
- Joint pains Arthralgias in Children
- Joint Swelling
- Joint/limit range of motion
- Knee manifestation/involvement/secondary
- Knee Pain
- Large joint involvement/manifestation
- Monoarticular Arthritis in Children
- Monoarticular Arthritis/One joint acute
- Single Joint Pain
- Skeletal problems/symptoms/signs
- Warm Joint
- Epistaxis Children
- Epistaxis, severe/persistent
- Asymmetric body/build
- Episodic symptoms/events
- Conjunctival/scleral hemorrhage
- Typical Clinical Presentation
- Females sicker than males/characteristic
- Clinical Presentation & Variations
- Presentation/Aggressive Osteoarthritis
- Presentation/Single Joint Arthritis
- Presentation/Painless Gross hematuria
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Recent Event
- Recent/Fall
- Recent/MVA
- Recent/Trauma
- Established Disease Population
- Patient/Hemophilia
- Population Group
- Child
- Man
- Population/Pediatrics population
- Young Adult
- Family History
- Family history/Bleeding disorders
- Family history/Blood disease
- Sex & Age Groups
- Population/Adult/all
- Population/Boy patient
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Population/Infant male
- Population/Male
- Population/Man patient
- Population/Young adult
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Chorionic Villous Sampling Abnormalities
- Chromosomal abnormality (Lab)
- Clotting factor assay/abnormal (Lab)
- Coagulation/Clotting factors decreased (Lab)
- DNATest specific/genetics laboratory/abnormality (Lab)
- PTT increased normal PT (Lab)
- URINE Dipstick /Blood abnormal
- Abnormal Lab Findings - Decreased
- Factor 8 (Lab)
- Transferrin saturation (Lab)
- Abnormal Lab Findings - Increased
- Clotting time/Activated clotting time test (Lab)
- Hepatitis B surface antigen positive (Lab)
- Platelet count (Lab)
- PTT/Partial Thromboplastin Time/Activated PTT (Lab)
- Recalcification time (Lab)
- Thromboplastin generation time (Lab)
- TIBC/Total Iron Binding capacity (Lab)
- URINE Red blood cells
- Diagnostic Test Results
- Other Tests & Procedures
- Amniocentesis/Abnormality
- ThromboElastoGram Abnormal (TEG)
- Angiography
- Arthrogram/knee many filling defects
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Abdominal wall/muscle hematoma
- Arthritis
- Bleeding complications/Surgery
- Bleeding diathesis/hemorrhagic diathesis
- Bleeding Tendency
- Cerebral hemorrhage
- Chronic hepatitis/Active
- Circulating anticoagulants disorder
- Circulating coagulation inhibitor status
- Epidural hematoma
- Epistaxis/nosebleed
- Gastrointestinal bleeding
- Hemarthrosis
- Hematomyelia
- Hemophilia
- Hemophilic arthritis
- Hemothorax
- Hepatitis, viral
- Hydronephrosis
- Internal bleeding/trauma
- Intestinal/bowel obstruction
- Intracerebral hematoma
- Iron deficiency anemia
- Jacksonian/posttraumatic epilepsy
- Muscle Hematoma
- Neck space/Hemorrhage/hematoma
- Osteoarthritis, degenerative
- Peptic ulcer hemorrhage
- Periostitis
- Peripheral neuropathy
- Polyneuritis
- Pseudogout (CPPD) arthritis
- Rectus Abdominus Hematoma
- Retroperitoneal hemorrhage
- Small bowel obstruction
- Subarachnoid hemorrhage
- Thrombocytosis
- Lower GI Bleeding/Infant
- Upper GI Bleeding in children
- Chronic Hepatitis
- Polyneuropathy
- Monoarthritis Acute
- Hematuria
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Hematologic (category)
- Pathophysiology
- Pathophysiology/Gene locus Chromosome X.
- Pathophysiology/Gene locus Chromosome Xq
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Gene locus Xq28
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Heterozygous/recessive silent/clinically
- Pathophysiology/Maternal inheritance
- Pathophysiology/Single gene locus indentified
- Process
- PROCESS/Enzyme defect/Metabolic disorder (ex)
- PROCESS/Hereditofamilial (category)
- PROCESS/Metabolic/storage disorder (category)
- PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
- PROCESS/Coagulation derangement/disorder (ex)
- PROCESS/Hereditary hemorrhagic/coagulation disorder (ex)
- Synonyms
- Synonym
- Synonym/AHG deficiency
- Synonym/Factor VIII deficiency
- Synonym/Hemophilia A
- Treatment
- Drug Therapy - Contraindication
- RX/Anticoagulants
- RX/Warfarin (Coumadin)
- Drug Therapy - Indication
- RX/Aminocaproic acid (Amicar)
- RX/Cryoprecipitate
- RX/Desmopressin (DDAVP)
- RX/Factor VIII IV Administration
- Other Treatments
- TX/Cultured Fibroblasts Infusion
- TX/Genetic counselling