Hallucinations
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
178
18
0.100
None
0
Elevated urinary delta-aminolevulinic acid
phenotype
Finding
3
1
0.100
None
0
1
Porphyria, Acute Intermittent, Nonerythroid Variant
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
1
2
0.100
None
0
2
Dysuria
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
17
3
0.100
None
0
1
Acute episodes of neuropathic symptoms
phenotype
Finding
4
3
0.100
None
0
2
Myalgia
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
226
22
0.100
None
0
Arthralgia
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Sign or Symptom
248
27
0.100
None
0
Cardiac Arrhythmia
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
559
111
0.100
None
0
Anxiety
disease
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
1048
287
0.100
None
0
2
Anorexia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
242
10
0.100
None
0
Paraparesis
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
31
5
0.100
None
0
Abnormal vision
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Finding
115
6
0.100
None
0
1
Constipation
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
424
57
0.100
None
0
1
Abdominal Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
302
18
0.100
None
0
3
Euthyroid Sick Syndromes
disease
Endocrine System Diseases
Disease or Syndrome
9
1
0.100
None
0
1
Diarrhea
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
632
63
0.100
None
0
1
Renal Insufficiency
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
615
42
0.100
None
0
Hyponatremia
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
109
11
0.100
None
0
1
Depressive disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1719
297
0.100
None
0
1
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
1
Acute intermittent porphyria
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
103
68
1.000
strong
0.983
173
60
1974
2020
Disorders of Porphyrin Metabolism
group
Nutritional and Metabolic Diseases
Disease or Syndrome
26
7
0.080
None
1.000
8
2
1978
2013
Hydroxymethylbilane Synthase Deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
2
0.310
None
1.000
3
1983
2013
Diabetes Mellitus, Experimental
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Experimental Model of Disease
522
0.200
None
1.000
1
1983
1983
Porphyrias, Hepatic
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
7
0.220
None
1.000
3
1984
2006