Uveal melanoma
|
disease |
Neoplasms; Eye Diseases
|
Neoplastic Process
|
8
|
15
|
0.800 |
None |
0.984 |
5 |
2
|
2008 |
2019 |
Sturge-Weber Syndrome
|
disease |
Neoplasms; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
1
|
0.800 |
None |
1.000 |
3 |
1
|
2013 |
2019 |
melanoma
|
disease |
Neoplasms
|
Neoplastic Process
|
248
|
212
|
0.700 |
None |
0.967 |
1 |
1
|
1989 |
2019 |
Port-Wine Stain
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
2
|
8
|
0.660 |
None |
1.000 |
1 |
1
|
2013 |
2020 |
Capillary malformation (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
2
|
2
|
0.660 |
limited |
0.833 |
0 |
1
|
2016 |
2020 |
Malignant melanoma of iris
|
disease |
Neoplasms; Eye Diseases
|
Neoplastic Process
|
5
|
|
0.410 |
None |
1.000 |
2 |
|
2010 |
2017 |
Malignant melanoma of choroid
|
disease |
Neoplasms; Eye Diseases
|
Neoplastic Process
|
5
|
3
|
0.400 |
None |
1.000 |
2 |
|
2010 |
2013 |
Congenital hemangioma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases
|
Neoplastic Process
|
2
|
|
0.330 |
moderate |
0.667 |
1 |
|
2016 |
2019 |
Port-wine stain with oculocutaneous melanosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases
|
Congenital Abnormality
|
2
|
|
0.320 |
None |
1.000 |
1 |
|
2016 |
2019 |
Craniofacial Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
156
|
|
0.300 |
None |
1.000 |
1 |
|
1998 |
1998 |
Nevi flammei, familial multiple
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Albuminuria
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Finding
|
24
|
59
|
0.300 |
None |
1.000 |
1 |
|
2005 |
2005 |
Hyalinosis, Segmental Glomerular
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
28
|
|
0.300 |
None |
1.000 |
1 |
|
2005 |
2005 |
Congenital Heart Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
44
|
18
|
0.300 |
None |
1.000 |
1 |
|
1998 |
1998 |
Focal glomerulosclerosis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
36
|
8
|
0.300 |
None |
1.000 |
1 |
|
2005 |
2005 |
Blood Coagulation Disorders
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
16
|
4
|
0.300 |
None |
1.000 |
1 |
|
1997 |
1997 |
Phakomatosis cesioflammea
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases
|
Congenital Abnormality
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Cutaneous Melanoma
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
41
|
195
|
0.300 |
None |
|
0 |
|
|
|