×
CUI:
C0027960
Disease:
Nevus
Nevus
disease
Neoplasms
Neoplastic Process
125
43
0.010
None
1.000
1
2000
2000
Melanocytic nevus
disease
Neoplasms
Neoplastic Process
297
33
0.010
None
1.000
1
2000
2000
Limb defects
group
Congenital Abnormality
67
2
0.010
None
1.000
1
1
2003
2003
Verruciform xanthoma of skin
disease
Nutritional and Metabolic Diseases
Neoplastic Process
2
0.010
None
1.000
1
2005
2005
Benign melanocytic nevus
disease
Neoplasms
Neoplastic Process
122
20
0.010
None
1.000
1
2000
2000
NEVUS, EPIDERMAL (disorder)
disease
Neoplasms
Disease or Syndrome
14
17
0.010
None
1.000
1
2019
2019
Skin lesion
group
Skin and Connective Tissue Diseases
Disease or Syndrome
563
52
0.020
None
1.000
2
2016
2019
Irritability, CTCAE
phenotype
Finding
140
0.100
None
0
Congenital absence of kidneys syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
110
0.100
None
0
Long face
phenotype
Finding
182
12
0.100
None
0
Narrow face
phenotype
Finding
87
6
0.100
None
0
Congenital exomphalos
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
235
0.100
None
0
Lumbar hyperlordosis
disease
Musculoskeletal Diseases
Anatomical Abnormality
92
8
0.100
None
0
Dysphasia
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
63
4
0.100
None
0
Hyperkeratosis
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
176
19
0.100
None
0
Nail abnormality
phenotype
Pathological Conditions, Signs and Symptoms
Anatomical Abnormality
67
11
0.100
None
0
Sleep Disorders
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
Mental or Behavioral Dysfunction
360
38
0.100
None
0
Dyssomnias
disease
Nervous System Diseases; Mental Disorders
Mental or Behavioral Dysfunction
236
10
0.100
None
0
Congenital Epicanthus
disease
Congenital Abnormality
417
30
0.100
None
0
Acquired Kyphoscoliosis
disease
Musculoskeletal Diseases
Acquired Abnormality
149
2
0.100
None
0
Microretrognathia
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
Finding
53
6
0.100
None
0
Mild intrauterine growth retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Finding
3
1
0.100
None
0
Hyperkeratosis, CTCAE
phenotype
Finding
87
0.100
None
0
Aplasia/hypoplasia of the extremities
disease
Congenital Abnormality
4
1
0.100
None
0
Almond-shaped palpebral fissure
phenotype
Finding
40
1
0.100
None
0