GLIOMA SUSCEPTIBILITY 1
|
phenotype |
|
Finding
|
6
|
14
|
0.400 |
None |
|
0 |
6
|
|
|
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
|
disease |
|
Finding
|
1
|
7
|
0.400 |
None |
|
0 |
7
|
|
|
BONE MARROW FAILURE SYNDROME 5
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.400 |
limited |
|
0 |
2
|
|
|
Benign tumor of pancreas
|
disease |
Digestive System Diseases; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
13
|
|
0.300 |
None |
|
0 |
|
|
|
Carcinoid tumor of intestine
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
4
|
|
0.300 |
strong |
|
0 |
|
|
|
Neoplasm of uncertain or unknown behavior of ovary
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Neoplastic Process
|
29
|
|
0.300 |
None |
|
0 |
|
|
|
Neoplasm of uncertain or unknown behavior of breast
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
41
|
|
0.300 |
None |
|
0 |
|
|
|
Carcinoma of Endocrine Gland
|
disease |
Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
22
|
|
0.300 |
strong |
|
0 |
|
|
|
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
|
disease |
Digestive System Diseases; Neoplasms
|
Disease or Syndrome
|
20
|
34
|
0.300 |
strong |
|
0 |
|
|
|
Neoplasms, Bone Tissue
|
group |
Neoplasms
|
Neoplastic Process
|
7
|
|
0.200 |
None |
|
0 |
|
|
|
Familial CHARGE Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
4
|
|
0.200 |
None |
|
0 |
|
|
|
Abdominal Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
302
|
18
|
0.100 |
None |
|
0 |
|
|
|
Anorexia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
242
|
10
|
0.100 |
None |
|
0 |
|
|
|
Back Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
110
|
10
|
0.100 |
None |
|
0 |
|
|
|
Cholestasis, Extrahepatic
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
87
|
|
0.100 |
None |
|
0 |
|
|
|
Chest Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
154
|
7
|
0.100 |
None |
|
0 |
|
|
|
Pathological fracture
|
phenotype |
Wounds and Injuries
|
Pathologic Function
|
35
|
2
|
0.100 |
None |
|
0 |
|
|
|
Congenital pectus excavatum
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
272
|
36
|
0.100 |
None |
|
0 |
1
|
|
|
Headache
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
338
|
75
|
0.100 |
None |
|
0 |
|
|
|
Hepatosplenomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases
|
Sign or Symptom
|
127
|
21
|
0.100 |
None |
|
0 |
|
|
|
Hyperaldosteronism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
84
|
6
|
0.100 |
None |
|
0 |
|
|
|
Hyperhidrosis disorder
|
phenotype |
Skin and Connective Tissue Diseases
|
Finding
|
114
|
7
|
0.100 |
None |
|
0 |
|
|
|
Hypertrichosis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
92
|
27
|
0.100 |
None |
|
0 |
|
|
|
Hypogonadism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
305
|
24
|
0.100 |
None |
|
0 |
|
|
|
Hypokalemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
61
|
7
|
0.100 |
None |
|
0 |
|
|
|