Disease Comparison Results (show all mode) for Meckel-Gruber syndrome and Weill-Marchesani syndrome

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Weill-Marchesani syndrome

Found: 28 | Differences: 18

Meckel-Gruber syndrome

Found: 59 | Differences: 49

Meckel-Gruber syndrome and Weill-Marchesani syndrome sharing 10 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Dysmorphic dwarfism/short stature
Dysmorphic appearance/face
Short stature
Short stature Child
Eye symptoms/signs
Small lens/congenital/sign
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Dwarfism
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Associated Diseases & Rule outs
Associated Disease & Complications
Congenital heart disease
Dwarfism
Nanism/dwarfism
Patent ductus arteriosis
Disease Mechanism & Classification
Class
CLASS/Ophthalmology Specialty Population
CLASS/Pediatric disorders (ex)
CLASS/Skeletal (category)
CLASS/Ophthalmology disorders
CLASS/Eye involvement/disorder (ex)
CLASS/Eyes/accessory (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Eponymic (category)
PROCESS/Hereditofamilial (category)
PROCESS/Multiple dysmorphic syndrome (ex)
Clinical Manifestations
Signs & Symptoms
Flat/Sloping forehead
Uvula anomaly/deformity
Bowing of extremities
Foot deformity
Sudden death of an infant
Narrow Palpebral Fissures
Clinical Presentation & Variations
Presentation/Kidney malformations Congenital syndrome Child
Disease Progression
Course/Chronic only
Course/Lethal
Demographics & Risk Factors
Ethnic or Racial Factors
Arab/population
Finnish population
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Diagnostic Test Results
Pathology
PATH/Occipital encephalocele/fetus
Associated Diseases & Rule outs
Associated Disease & Complications
Cataract
Cleft Lip
Cleft lip/deformity
Cleft palate/deformity
Clubbed foot/congenital
Congenital anomalies
Death Newborn/Perinatal
Genital anomalies/caused
Infantile Polycystic kidney disease
Limb deformities/anomalies
Meckel-Gruber syndrome
Meningoencephalocele
Microcephaly/oligophrenia
Microphthalmos
Polycystic kidney disease
Polydactyly/Supernumery digits
Recurrent GI Bleeding
Renal cyst
Stillborn
Sudden death/Child
Hand anomalies
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Fetal/conceptual products (category)
CLASS/Intestinal/stomach/gut (category)
Pathophysiology
Pathophysiology/Gene locus chromosome 12
Pathophysiology/Gene locus chromosome 12q
Pathophysiology/Gene locus Chromosome 17q
Pathophysiology/Gene locus Chromosome 8q
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/MKS1 Gene Mutation
Pathophysiology/MKS2 Gene Mutation
Pathophysiology/Gene locus chromosome 8
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/Anomalies/Deformities/Malformations (EX)
PROCESS/Lethal perinatal/Incompatible with survival
Synonyms
Synonym
Synonym/Dysencephalia splanchnocystica
Synonym/Meckel syndrome
Treatment
Other Treatments
TX/Genetic counselling
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