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- Disease Information
- Disease Comparison
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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
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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 differences mode) for Familial progressive polyneuropathy and Laurence-Moon-Biedel syndrome
Found: 76 | Differences: 67
Familial progressive polyneuropathy
Found: 29 | Differences: 20Familial progressive polyneuropathy and Laurence-Moon-Biedel syndrome sharing 9 common findings. (show all, show common, show differences)
- Clinical Manifestations
- Signs & Symptoms
- Delayed male adolescence/pubescence
- Genital Hypoplasia/Male
- Penis, small (Micropenis)
- Scrotum small
- Undescended testicles
- Mental Deficiency Child
- Weight gain
- Bilateral Vision Loss
- Narrow Palpebral Fissures
- Visual Problems
- Clinical Presentation & Variations
- Presentation/Obese Retarded Blind Hypogenital male Youth
- Presentation/Congenital Syndromes Renal failure
- Presentation/Juvenile Cataract
- Demographics & Risk Factors
- Family History
- Family history/Parental consanguinity
- Sex & Age Groups
- Population/Child-Infant Only
- Population/Male
- Laboratory Tests
- Abnormal Lab Findings - Decreased
- FSH/Follicle Stmulating Hormone/ICSH (Lab)
- LH/Leutinizing Hormone (Lab)
- Testosterone Total (Lab)
- Diagnostic Test Results
- Other Tests & Procedures
- TEST/Failure of clomiphen to raise FSH/LH
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Prader-Willi syndrome
- Associated Disease & Complications - Causes
- Blindness
- Blindness, central
- Cataract
- Congenital heart disease
- Congenital urinary tract malformations
- Hereditary Blindness
- Hypogenitalism/male
- Hypogonadism, male
- Infertility/sterility male
- Laurence-Moon syndrome
- Limb deformities/anomalies
- Mental retardation
- Microphallus deformity
- Microphthalmos
- Obesity
- Obesity in Children
- Obesity, massive
- Paraplegia, spastic
- Paraplegia, spastic hereditary
- Pigmentary retinal dystrophy
- Polydactyly/Supernumery digits
- Renal anomalies
- Renal Failure Chronic
- Retinal Degeneration/Dystrophy
- Retinitis pigmentosa
- Retinopathy
- Secondary male hypogonadism
- Skull deformities
- Strabismus, convergent
- Tetralogy of Fallot
- Genital Hypoplasia
- Hand anomalies
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Systemic/no comment (category)
- Pathophysiology
- Pathophysiology/Gene locus Chromosome 16
- Pathophysiology/Gene locus Chromosome 16q
- Pathophysiology/Novel Gene BBS/LMB at 16q
- Pathophysiology/Hypogonadotrophic hypogonadism
- Pathophysiology/Secondary Testicular Failure
- Pathophysiology/Hypothalamic pituitary dysfunction
- Process
- PROCESS/Autosomal recessive disorder (ex)
- PROCESS/Hypogonadotropic hypogonadism/congenital
- Synonyms
- Synonym
- Synonym/Bardet-Biedl syndrome
- Clinical Manifestations
- Signs & Symptoms
- Symmetrical muscle/pain, weakness
- Bilateral foot drop/signs
- Neurological symptoms/signs
- Paresthesias
- Symmetric Polyneuropathy
- Clinical Presentation & Variations
- Presentation/Progressive Motor Sensory Polyneuropathy
- Diagnostic Test Results
- Pathology
- BX/Nerve biopsy/abnormal
- Electrodiagnosis
- EMG/NCA Low amplitude
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Diabetic peripheral neuropathy
- Peroneal muscular atrophy/Charcot Marie Tooth
- Associated Disease & Complications - Causes
- Polyneuritis
- Disease Mechanism & Classification
- Class
- CLASS/Neurologic (category)
- CLASS/Peripheral nerve disease (ex)
- Pathophysiology
- Pathophysiology/Gene locus 12q24
- Pathophysiology/Gene locus 12q24-qter
- Pathophysiology/Gene locus chromosome 12
- Pathophysiology/Hereditary disease/Adult manifestations
- Pathophysiology/Hereditary Neuropathy
- Treatment
- Drug Therapy
- SX/Nerve biopsy
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