PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
|
disease |
Digestive System Diseases; Neoplasms
|
Disease or Syndrome
|
6
|
33
|
0.300 |
strong |
|
0 |
|
|
|
GLIOMA SUSCEPTIBILITY 1
|
phenotype |
|
Finding
|
6
|
14
|
0.400 |
None |
|
0 |
6
|
|
|
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 |
|
|
|
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
|
disease |
|
Finding
|
1
|
7
|
0.400 |
None |
|
0 |
7
|
|
|
Carcinoid tumor of intestine
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
4
|
|
0.300 |
strong |
|
0 |
|
|
|
Carcinoma of Endocrine Gland
|
disease |
Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
15
|
|
0.300 |
strong |
|
0 |
|
|
|
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 |
|
|
|
Neoplasm of uncertain or unknown behavior of breast
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
41
|
|
0.300 |
None |
|
0 |
|
|
|
Penile Neoplasms
|
group |
Neoplasms; Male Urogenital Diseases
|
Neoplastic Process
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1998 |
1998 |
Pustulosis of Palms and Soles
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
57
|
|
0.300 |
None |
1.000 |
1 |
|
1999 |
1999 |
Thymus Neoplasms
|
group |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
4
|
1
|
0.510 |
None |
1.000 |
0 |
|
1998 |
2000 |
ADRENOCORTICAL CARCINOMA, HEREDITARY
|
disease |
Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
1
|
6
|
0.620 |
None |
1.000 |
0 |
6
|
1994 |
2001 |
Paraganglioma
|
disease |
Neoplasms
|
Neoplastic Process
|
13
|
10
|
0.310 |
strong |
1.000 |
0 |
|
2003 |
2003 |
Chromosome 17 deletion
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Cell or Molecular Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2004 |
2004 |
Chromosome 17p Deletion Syndrome
|
phenotype |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Cell or Molecular Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2004 |
2004 |
Carcinomatosis
|
phenotype |
Neoplasms
|
Neoplastic Process
|
163
|
|
0.300 |
None |
1.000 |
2 |
|
1998 |
2007 |
Chronic Airflow Obstruction
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
33
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Carotid Artery Diseases
|
group |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
11
|
|
0.310 |
None |
1.000 |
1 |
|
2007 |
2007 |
Amyotrophic Lateral Sclerosis, Guam Form
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
31
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Vulvar Lichen Sclerosus
|
disease |
Female Urogenital Diseases and Pregnancy Complications
|
Disease or Syndrome
|
2
|
|
0.310 |
None |
1.000 |
1 |
|
2002 |
2007 |
Amyotrophic Lateral Sclerosis With Dementia
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
29
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
External Carotid Artery Diseases
|
group |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
11
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Internal Carotid Artery Diseases
|
group |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
11
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Arterial Diseases, Common Carotid
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
11
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |