Abnormal cochlea morphology
disease
Anatomical Abnormality
16
1
0.100
None
0
Abnormality of the clavicle
disease
Anatomical Abnormality
42
0.100
None
0
Abnormality of the gingiva
disease
Anatomical Abnormality
13
1
0.100
None
0
Abnormality of the helix
phenotype
Finding
21
2
0.100
None
0
Abnormality of the nasopharynx
disease
Anatomical Abnormality
10
0.100
None
0
Abnormality of the stapes
disease
Anatomical Abnormality
1
0.100
None
0
Abnormality of the ureter
phenotype
Finding
19
0.100
None
0
Absent speech
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
232
72
0.100
None
0
×
CUI:
C0702166
Disease:
Acne
Acne
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
167
11
0.010
None
1.000
1
2019
2019
Acne Vulgaris
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
94
37
0.010
None
1.000
1
2019
2019
Acquired Camptodactyly
disease
Acquired Abnormality
120
1
0.100
None
0
Acquired Kyphoscoliosis
disease
Musculoskeletal Diseases
Acquired Abnormality
149
2
0.100
None
0
Acute myelomonocytic leukemia
disease
Neoplasms
Neoplastic Process
105
3
0.010
None
1.000
1
2018
2018
Acute Undifferentiated Leukemia
disease
Neoplastic Process
119
1
0.010
None
< 0.001
1
2007
2007
Adult Myelodysplastic Syndrome
disease
Hemic and Lymphatic Diseases
Neoplastic Process
332
20
0.020
None
1.000
2
2014
2018
Alacrima
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Disease or Syndrome
16
1
0.100
None
0
Alopecia
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
491
375
0.100
None
1.000
1
1
2017
2017
Androgen-Insensitivity Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Disease or Syndrome
247
176
0.010
None
1.000
1
2015
2015
Annular pancreas
disease
Digestive System Diseases
Congenital Abnormality
19
1
0.100
None
0
Anteriorly placed anus
phenotype
Finding
34
5
0.100
None
0
Anteverted nostril
phenotype
Finding
407
35
0.100
None
0
Aplasia/Hypoplasia of the pubic bone
phenotype
Finding
2
0.100
None
0
Arnold-Chiari Malformation, Type I
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
41
1
0.100
None
0
Arthrogryposis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
198
33
0.100
None
1.000
1
1
2020
2020
Asthma
disease
Respiratory Tract Diseases; Immune System Diseases
Disease or Syndrome
2096
1536
0.010
None
1.000
1
2017
2017