Lipidemias
phenotype
Nutritional and Metabolic Diseases
Finding
18
0.300
None
1.000
1
1977
1977
Hypocalciuric hypercalcemia, familial, type 1
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
46
58
0.010
None
1.000
1
1977
1977
Turner Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases
Disease or Syndrome
162
21
0.010
None
1.000
1
1979
1979
Gonadal Dysgenesis, 45,X
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases
Disease or Syndrome
23
0.010
None
1.000
1
1979
1979
Ciliary Body Spasm
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
2
0.300
None
1.000
1
1980
1980
Generalized Spasms
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
2
0.300
None
1.000
1
1980
1980
Sinus Tachycardia
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
29
5
0.300
None
1.000
1
1980
1980
×
CUI:
C0037763
Disease:
Spasm
Spasm
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
172
9
0.300
None
1.000
1
1980
1980
Exogenous Hyperinsulinism
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
26
0.300
None
1.000
1
1986
1986
Endogenous Hyperinsulinism
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
26
0.300
None
1.000
1
1986
1986
Autoimmune Diseases
group
Immune System Diseases
Disease or Syndrome
1758
428
0.010
None
1.000
1
1986
1986
Compensatory Hyperinsulinemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
30
2
0.300
None
1.000
1
1986
1986
Glycogen Storage Disease Type VI
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
15
22
0.010
None
1.000
1
1987
1987
Adenomatous Polyposis Coli
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
Neoplastic Process
609
237
0.010
None
1.000
1
1991
1991
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
74
68
0.010
None
1.000
1
1991
1991
Hypotension
phenotype
Cardiovascular Diseases
Finding
125
2
0.300
None
1.000
2
1988
1993
Myocardial Failure
disease
Cardiovascular Diseases
Disease or Syndrome
119
0.300
None
1.000
1
1995
1995
Left-Sided Heart Failure
disease
Cardiovascular Diseases
Disease or Syndrome
123
5
0.300
None
1.000
1
1995
1995
Heart Decompensation
phenotype
Cardiovascular Diseases
Pathologic Function
113
0.300
None
1.000
1
1995
1995
Tachyarrhythmia
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Finding
18
0.300
None
1.000
1
1995
1995
Heart Failure, Right-Sided
disease
Cardiovascular Diseases
Disease or Syndrome
154
0.300
None
1.000
1
1995
1995
Tachycardia
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Finding
73
8
0.300
None
1.000
1
1995
1995
Pachyonychia Congenita, Jadassohn Lewandowsky Type
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Disease or Syndrome
8
19
0.010
None
1.000
1
1996
1996
Meningioma
disease
Neoplasms; Nervous System Diseases
Neoplastic Process
634
43
0.010
None
1.000
1
1997
1997
Bradycardia
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Finding
63
2
0.300
None
1.000
5
1984
1998