ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.730 |
strong |
1.000 |
4 |
6
|
2010 |
2018 |
Ectodermal dysplasia syndactyly syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
1
|
|
0.030 |
None |
1.000 |
3 |
|
2010 |
2015 |
Absent facial hair
|
phenotype |
|
Congenital Abnormality
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Simple syndactyly of toes, first web space
|
disease |
|
Congenital Abnormality
|
5
|
3
|
0.100 |
None |
|
0 |
|
|
|
Palmar hyperkeratosis
|
disease |
|
Disease or Syndrome
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Patchy alopecia
|
phenotype |
Skin and Connective Tissue Diseases
|
Finding
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Distemper
|
disease |
Infections; Animal Diseases
|
Disease or Syndrome
|
12
|
|
0.040 |
None |
1.000 |
4 |
|
2014 |
2017 |
Pili Torti
|
phenotype |
Skin and Connective Tissue Diseases
|
Finding
|
12
|
|
0.100 |
None |
|
0 |
|
|
|
Peg-shaped teeth
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
17
|
2
|
0.100 |
None |
|
0 |
|
|
|
Cutaneous finger syndactyly
|
disease |
|
Congenital Abnormality
|
20
|
1
|
0.100 |
None |
|
0 |
|
|
|
Poliomyelitis
|
disease |
Infections; Nervous System Diseases
|
Disease or Syndrome
|
23
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Metastatic urothelial carcinoma
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Neoplastic Process
|
28
|
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2019 |
Hypoplastic toenails
|
phenotype |
|
Finding
|
42
|
1
|
0.100 |
None |
|
0 |
|
|
|
Subacute Sclerosing Panencephalitis
|
disease |
Infections; Nervous System Diseases
|
Disease or Syndrome
|
47
|
6
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Coarse hair
|
phenotype |
|
Finding
|
60
|
4
|
0.100 |
None |
|
0 |
|
|
|
Sparse eyelashes
|
phenotype |
|
Finding
|
60
|
4
|
0.100 |
None |
|
0 |
|
|
|
Sparse and thin eyebrow
|
phenotype |
|
Finding
|
68
|
8
|
0.100 |
None |
|
0 |
|
|
|
Ectodermal Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
71
|
16
|
0.130 |
None |
1.000 |
3 |
|
2011 |
2018 |
Widely spaced teeth
|
phenotype |
|
Finding
|
71
|
10
|
0.100 |
None |
|
0 |
|
|
|
Dental Enamel Hypoplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Disease or Syndrome
|
72
|
1
|
0.100 |
None |
|
0 |
|
|
|
Sparse scalp hair
|
phenotype |
|
Finding
|
85
|
7
|
0.100 |
None |
|
0 |
|
|
|
Luminal B Breast Carcinoma
|
disease |
|
Neoplastic Process
|
103
|
7
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Measles
|
disease |
Infections
|
Disease or Syndrome
|
113
|
6
|
0.070 |
None |
1.000 |
7 |
|
2011 |
2018 |
High grade serous carcinoma
|
disease |
|
Neoplastic Process
|
118
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Cleft palate with cleft lip
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
|
Congenital Abnormality
|
119
|
43
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |