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Disease Comparison Results (show all mode) for Goldenhar syndrome and Intestinal/gut lymphoma

Clinical
Demographics
Lab
Diagnostic
Diseases
Classification
Synonyms
Treatment
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Intestinal/gut lymphoma

Found: 180 | Differences: 178

Goldenhar syndrome

Found: 135 | Differences: 133

Goldenhar syndrome and Intestinal/gut lymphoma sharing 2 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Abdominal Distension; Abdominal Distension in Children; Abdominal distension/protrusion/sign; Abdominal Distention; Abdominal Mass; Abdominal Mass in Children; Abdominal Mass in Elderly; Abdominal Pain; Abdominal pain after meals/eating food; Abdominal Pain in Adolescent; Abdominal Pain in Children; Abdominal pain/triggered by alcohol; Abdominal paresthesias; Abdominal tenderness; Active Bowel Sounds; Alcohol drinking intolerance/new; Anorexia Decreased appetite; Beer drinking intolerance; Borborygmi/Bowel sound increased; Bowel sounds high pitched; Chronic Abdominal Pain; Cibaphobia/Fear of Eating; Constipation in Elderly; Diarrhea; Diarrhea and Weight Loss; Diarrhea, chronic; Epigastric mass; Fatty food intolerance; Fatty stools/Fecal fat /Greasy stool; Hypereactive Bowel Sounds; Increased abdominal girth/Potbelly; Nocturnal abdominal pain; Protruberant Abdomen; Recurrent Abdominal Pain; Rigid Abdomen in Children; Thickened bowel loops palpable/Abdomen; Vague GI symptoms/persistent; Hepatosplenomegaly; Palpable Liver/Hepatomegaly; Right Flank Mass; Flank Mass; Left Flank Mass; Splenomegaly; Fatigue Tiredness in Elderly; Fever; Fever Febrile Possible; Fever of unknown origin/chronic fever; Flu-Like Syndrome; High body temperature; Malaise; Weight Loss
Clinical Presentation & Variations: Presentation/Intussusception Bowel Older Child
Disease Progression: Course/Chronic disorder; Course/Chronic only

Demographics & Risk Factors
Ethnic or Racial Factors: Arab/population; Middle Eastern Population; Saudi Arabian population; Sephardic Jewish population
Established Disease Population: Patient/Sprue/gluten enteropathy; Patient/Lymphoma, malignant, non-Hodgkins
Sex & Age Groups: Population/Adult Aged Only; Population/Adult/all; Population/Male; Population/Sixties-adult

Laboratory Tests
Abnormal Lab Findings (Non Measured): Acute inflammatory markers elevated (Lab); Macrocytosis/smear (Lab); Fecal Globin Immunochemical Test positive
Abnormal Lab Findings - Decreased: Albumin, serum (Lab); Total Protein, serum (Lab); Vitamin B12, serum (Lab)
Abnormal Lab Findings - Increased: Lactic Dehydrogenase (LDH LH) (Lab); MCV/Mean Corpuscular Volume (Lab); Uric acid, serum (Lab); STOOL Alpha-trypsin/quantitative; STOOL/Osmolar gradient Above 120

Diagnostic Test Results
Other Tests & Procedures: Laparoscopy/Abdominal abnormal; TEST/D-Xylose absorption abnormal
Pathology: BX/Intestinal biopsy/ileum/ abnormal; BX/Intestinal biopsy/Jejunal/Abnormal
Isotope Scan: Isotope/Schilling Test/B12 isotope/Abnormal
CT Scan: CT Scan/Abdomen Cecum lesion; CT Scan/Abdomen Mesenteric mass; CT Scan/Abdomen Retroperitoneal lymphadenopathy; CT Scan/CTA Abdomen Abnormal; CT Scan/Mesenteric adenopathy/ABD; CT Scan/Thickened bowel wall/ABD; CT Scan/Thickened/small-bowel wall/ABD; CT/Enterography Abnormal; MRI/MRA Abomen Abnormal
X-RAY: Xray/Encasing 'sandwich' mass mesenteric vessels/fat/loops/ABD
X-RAY With contrast: BE/Colon thumbprinting mucosa (Xray); BE/Lesion of cecum (Xray); SBS/Abnormal Small Bowel Series; SBS/Bulls-eye lesion/gut; SBS/Intestinal nodular filling defect (Xray); SBS/Mucosal destruction small bowel (Xray); SBS/Mucosal folds thickened, intestinal (Xray); SBS/Multiple intramural/bowel wall small nodules (Xray); SBS/Multiple nodules/intestinal (Xray); SBS/Separation bowel loops (Xray); SBS/Small bowel mass (Xray); SBS/Valvulae conniventes thickened (Xray); UGI/Duodenum external pressure deformity; UGI/Duodenum mass/intrinsic; UGI/Duodenum thickened folds; UGI/Duodenum widened loop; UGI/Postbulbar-jejunal ulceration

Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs: AIDS Wasting Disease; Autoimmune Pancreatitis; Crohn's disease (regional enteritis); Lactose intolerance syndrome; Sprue (gluten enteropathy); Ulcerative colitis; Whipple's disease
Associated Disease & Complications - Causes: Abdominal lymphatics obstruction/Cysterna ch.; Ascites; Ascites in Children; Bowel stricture; Chylous ascites; Constipation; Duodenal Stenosis; Gastric lymphoma; Hyperuricemia; Hypoalbuminemia Hypoproteinemia; Hypovitaminosis B12; Incomplete small bowel ostruction; Intestinal/Bowel Obstruction in Elderly; Intestinal/bowel obstruction; Intestinal/gut lymphoma; Jejunal ulceration; Lymphoma of colon; Lymphoma/Malignant lymphoma; Lymphoproliferative disorder; Malabsorption/Steatorrhea syndrome; Megaloblastic anemia/disease; Mesenteric adenitis; Obstipation; Peritoneal Effusion; Peritonitis. acute; Protein losing enteropathy; Retroperitoneal tumor; Short-bowel syndrome; Small bowel obstruction; Steatorrhea; Vitamin B12 deficiency; Lower GI bleeding; Small Intestine Bleeding

Disease Mechanism & Classification
Class: CLASS/Hematologic (category); CLASS/Leukocyte involvement/disorder (ex); CLASS/Intestinal disorder (ex); CLASS/Intestinal/stomach/gut (category); CLASS/Lymphatics/lymph (category); CLASS/Lymphocyte disorder (ex); CLASS/Spleen/thymus/RES/immune system (category)
Pathophysiology: Pathophysiology/Infiltrative process; Pathophysiology/B12 Intrinsic Factor receptors dys; Pathophysiology/Iron Malabsorption; Pathophysiology/Fat Malabsorption; Pathophysiology/Fat soluble Vitamin Malabsorption; Pathophysiology/Ileal absorption impaired; Pathophysiology/Ileum involvement/disorder; Pathophysiology/Inadequate absorptive area small bowel; Pathophysiology/Intermittant partial bowel obstruction; Pathophysiology/Malabsorption; Pathophysiology/Peristalsis increased; Pathophysiology/Small bowel bleeding source/adults
Process: PROCESS/Gastrointestinal malignancy/Cancer (ex); PROCESS/Lymphomas (ex); PROCESS/Malignancy/cancer (ex); PROCESS/Neoplastic (category); PROCESS/Lymphoproliferative disorder (ex); PROCESS/GI Tumors (all); PROCESS/GI tumors/children (ex)

Synonyms
Synonym: Synonym/Lymphoma, intestine/gut; Synonym/Lymphosarcoma, small intestine; Synonym/Small Intestinal/gut lymphoma

Treatment
Drug Therapy: RX/Chemotherapy(cancer); SX/Laparotomy
Surgical Procedures or Treatments: SX/Surgery

Clinical Manifestations
Signs & Symptoms: Particular physiognomy/Odd looking kids; Congenital facial deformities; Craniofacial Abnormalities/Congenital; Facial Asymmetry; Facial hemihypertrophy; Sunken Cheek Bones; Feeding/swallowing difficulties/infant; Large mouth/macrostomia; Receding chin deformity; Facial Nerve Palsy/Facial Paralysis; Facial weakness/droop, unilateral; Mental Deficiency Child; Asymmetric Limbs; Cranial asymmetry; Hypoplastic thumb deformity; Difficult intubations/anatomic; Snoring; Lateral Asymmetry; Eye symptoms/signs; Low set/odd position ears
Typical Clinical Presentation: Facies/Asymmetric/pinna/microphthalmic/micrognathia/macrosomia
Clinical Presentation & Variations: Presentation/Multiple deformities newborn (odd look)
Disease Progression: Course/Chronic disorder; Course/Chronic only

Demographics & Risk Factors
Population Group: Child; Population/Pediatrics population
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all

Diagnostic Test Results
CT Scan: CT Scan/Head Brain Arachnoid/epidermoid cyst; CT Scan/Head Brain/Corpus callosum hypoplasia/agenesis
X-RAY: Xray/Zygoma abnormality; Xray/Absent/hypoplastic radius bones; Xray/Atlas occipitalization/deformity/Skull

Associated Diseases & Rule outs
Associated Disease & Complications: Airway obstruction/Children; Aortic arch congenital anomalies; Arnold-Chiari syndrome; Bells palsy/Facial nerve paralysis; Coarctation of aorta; Congenital heart disease; Congenitally fused cervical vertebrae; Corpus callosum defect/agenesis; Deafness; Deafness, congenital; Deformities/5p deletion syndrome; Dextrocardia; Ear deformities/congenital; Eye Anomalies; Facial dysplasia; Facial nerve palsy/secondary; Facial paralysis of newborn; Goldenhar syndrome; Hemihypertrophy; Hydrocephalus; Hydronephrosis; Hydroureter/congenital; Hypoplastic Zygomatic Arch; Klippel-Feil syndrome; Limb deformities/anomalies; Lung anomaly/hypoplasia; Mental retardation; Micrognathia/congenital small chin; Multiple Congenital Anomalies; Multiple congenital anomalies/Mental retardation; Platybasia; Pulmonic valve stenosis; Renal anomalies; Renal anomaly/aplasia/hypoplasia; Situs inversus; Sleep apnea syndrome; Spina bifida; Spina bifida occulta; Spinal anomaly, congenital; Talipes varus deformity; Tetralogy of Fallot; Tracheo-esophageal fistula, congenital; Transposition great vessels; Vertebrae Anomalies; Vertebral anomalies; Facial Paralysis; Hand anomalies; Hereditary Deafness/Sensorineural

Disease Mechanism & Classification
Class: CLASS/Jablonski/NIH Archive Anomalies Database; CLASS/Pediatric disorders (ex); CLASS/Faces-cranio online database (ex); CLASS/Skeletal (category); CLASS/Eye involvement/disorder (ex)
Pathophysiology: Pathophysiology/Asymmetric deformities; Pathophysiology/Chromosome 7 gene defect; Pathophysiology/Chromosome gene/segment deletion (ex); Pathophysiology/Chromosome-5 involvement; Pathophysiology/Gene locus Chromosome 18; Pathophysiology/Gene locus chromosome 21; Pathophysiology/Gene locus chromosome 22; Pathophysiology/Gene locus Chromosome 5p; Pathophysiology/Gene locus Chromosome 6; Pathophysiology/Gene locus Chromosome 6q; Pathophysiology/Gene locus Chromosome 7; Pathophysiology/Gene locus Chromosome 9; Pathophysiology/Sporadic/hereditary/process; Pathophysiology/Corpus callosum defect; Pathophysiology/Maternal Chromosome mutation; Pathophysiology/Postaxial limb deficiency/phocomelia; Pathophysiology/Hereditary deafness; Pathophysiology/Gene locus chromosome 8
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Congenital/developmental (category); PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Esoteric disease (example); PROCESS/INCIDENCE/Rare disease (ex); PROCESS/Dystostosis/craniofacial (ex)

Synonyms
Synonym: Synonym/Auriculobranchiogenital dysplasia; Synonym/Dysplasia Oculo-auricularis; Synonym/Facio-Auriculovertebral malformation; Synonym/First and second Branchial arch syndrome; Synonym/First arch syndrome; Synonym/Franceschetti-Goldenhar Syndrome; Synonym/Goldenhar-Gorlin Syndrome; Synonym/Hemifacial microsomia; Synonym/Hemignathia and microtia syndrome; Synonym/Intrauterine facial necosis variant; Synonym/Lateral facial dysplasia; Synonym/Mandibulofacial dysostosis with epibulbar dermoids; Synonym/Necrotic facial dysplasia Variant; Synonym/Oculoauriculvertebral dysplasia syndrome; Synonym/Oromandibular-otic syndrome; Synonym/Otofacial dysostosis; Synonym/Otomandibular facial dysmorphogenesis; Synonym/Otomandibular syndrome; Synonym/Unilateral craniofacial microsomia; Synonym/Unilateral Intrauterine facial necrosis; Synonym/Unilateral Mandibulofacial dysostosis

Treatment
Drug Therapy: SX/Plastic/Facial Surgery

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