SERPING1, serpin family G member 1, 710

N. diseases: 207; N. variants: 43
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0023052
Disease: Laryngeal Edema
Laryngeal Edema
phenotype Respiratory Tract Diseases; Otorhinolaryngologic Diseases Pathologic Function 1 0.100 None 0
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 0.100 None 0
CUI: C4025190
Disease: Abnormal epiglottis morphology
Abnormal epiglottis morphology
phenotype Anatomical Abnormality 2 1 0.100 None 0
CUI: C4021978
Disease: Abnormality of salivation
Abnormality of salivation
phenotype Finding 3 1 0.100 None 0
CUI: C4021777
Disease: Abnormality of the larynx
Abnormality of the larynx
phenotype Anatomical Abnormality 11 1 0.100 None 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
group Digestive System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 389 50 0.100 None 0
COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR
disease Finding 1 1 0.100 None 0 1
CUI: C0019825
Disease: Hoarseness
Hoarseness
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Sign or Symptom 84 3 0.100 None 0
CUI: C0542571
Disease: Facial edema
Facial edema
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases; Cardiovascular Diseases Pathologic Function 9 1 0.100 None 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 8 2 0.100 None 0
CUI: C2732374
Disease: Edema of dorsum of hand
Edema of dorsum of hand
phenotype Pathological Conditions, Signs and Symptoms Finding 9 0.100 None 0
CUI: C0011991
Disease: Diarrhea
Diarrhea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 632 63 0.100 None 0
CUI: C0343065
Disease: Dermatographic urticaria
Dermatographic urticaria
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 12 1 0.100 None 0
CUI: C4025885
Disease: Abnormality of the uvula
Abnormality of the uvula
phenotype Anatomical Abnormality 2 2 0.100 None 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration
phenotype Finding 17 0.100 None 0
CUI: C0151610
Disease: Edema of the tongue
Edema of the tongue
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Stomatognathic Diseases; Cardiovascular Diseases Pathologic Function 1 0.100 None 0
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.100 None 0
CUI: C1142262
Disease: Intestinal edema
Intestinal edema
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 2 0.100 None 0
CUI: C0002994
Disease: Angioedema
Angioedema
phenotype Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Pathologic Function 18 8 0.100 None 0 2
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy
disease Nervous System Diseases Disease or Syndrome 94 12 0.100 None 0
CUI: C4476719
Disease: Limbal edema
Limbal edema
phenotype Pathologic Function 1 0.100 None 0
CUI: C0236024
Disease: Edema of pharynx
Edema of pharynx
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases Pathologic Function 2 0.100 None 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 121 8 0.100 None 0
CUI: C0027497
Disease: Nausea
Nausea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 161 14 0.100 None 0
CUI: C0004368
Disease: Autoimmune state
Autoimmune state
phenotype Pathologic Function 70 0.100 None 0