Tumor Cell Invasion
phenotype
Neoplastic Process
6626
169
0.090
None
1.000
9
2013
2019
INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL
disease
Disease or Syndrome
1
6
0.720
None
1.000
5
6
2012
2018
EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE
disease
Disease or Syndrome
2
0.300
strong
1.000
2
2012
2015
Malignant neoplasm of colon and/or rectum
disease
Neoplastic Process
3669
502
0.020
None
1.000
2
2015
2018
Macrotia
disease
Congenital Abnormality
188
18
0.100
None
0
Round face
phenotype
Finding
88
3
0.100
None
0
Fragile skin
phenotype
Finding
26
5
0.100
None
0
Fine hair
phenotype
Finding
69
1
0.100
None
0
Large nose
phenotype
Finding
70
7
0.100
None
0
Narrow thorax
phenotype
Finding
112
18
0.100
None
0
Decreased glomerular filtration rate
phenotype
Finding
11
0.100
None
0
Prominent forehead
phenotype
Finding
159
25
0.100
None
0
Sparse eyelashes
phenotype
Finding
60
4
0.100
None
0
Sparse scalp hair
phenotype
Finding
85
7
0.100
None
0
Tubular atrophy
phenotype
Finding
17
1
0.100
None
0
Abnormal blistering of the skin
phenotype
Finding
75
10
0.100
None
0
Sparse and thin eyebrow
phenotype
Finding
68
8
0.100
None
0
Tubular Atrophy Assessment
phenotype
Diagnostic Procedure
17
0.100
None
0
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
Disease or Syndrome
1410
80
0.020
None
1.000
2
2019
2020
×
CUI:
C1968949
Disease:
Cakut
Cakut
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
72
8
0.010
None
1.000
1
2014
2014
Opitz GBBB Syndrome, X-Linked
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Stomatognathic Diseases
Disease or Syndrome
79
24
0.010
None
1.000
1
2019
2019
Craniosynostosis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
488
90
0.010
None
1.000
1
2018
2018
Orbital separation excessive
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
590
77
0.100
None
0
Microcephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Congenital Abnormality
1064
27
0.100
None
0
Neural Tube Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
304
122
0.010
None
1.000
1
2013
2013