Abnormal lung lobation
disease
Respiratory Tract Diseases
Congenital Abnormality
32
0.100
None
0
Abnormal pigmentation
phenotype
Finding
58
5
0.100
None
0
Abnormality of immune system physiology
phenotype
Pathologic Function
42
1
0.100
None
0
Abnormality of vision
disease
Finding
127
8
0.100
None
0
Acute lymphocytic leukemia
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1293
222
0.010
None
1.000
1
2002
2002
Adenocarcinoma
group
Neoplasms
Neoplastic Process
2235
168
0.030
None
1.000
3
2000
2017
Adenoid Cystic Carcinoma
disease
Neoplasms
Neoplastic Process
325
30
0.010
None
1.000
1
2006
2006
Adenoma
group
Neoplasms
Neoplastic Process
1183
103
0.020
None
1.000
2
2008
2008
Adult Giant Cell Glioblastoma
disease
Neoplasms
Neoplastic Process
13
3
0.010
None
1.000
1
2001
2001
Adult Glioblastoma
disease
Neoplasms
Neoplastic Process
2528
98
0.030
None
1.000
3
2001
2019
Adult Lymphoma
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1169
66
0.010
None
1.000
1
2002
2002
Adult T-Cell Lymphoma/Leukemia
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
540
11
0.010
None
1.000
1
2000
2000
Ambiguous Genitalia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Congenital Abnormality
109
14
0.100
None
0
Anaplastic thyroid carcinoma
disease
Neoplasms
Neoplastic Process
392
16
0.010
None
1.000
1
2008
2008
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
Disease or Syndrome
1410
80
0.010
None
1.000
1
2019
2019
Aortic coarctation
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
88
6
0.100
None
0
Aortic Valve Insufficiency
disease
Cardiovascular Diseases
Disease or Syndrome
377
8
0.100
None
0
Aplasia/Hypoplasia of the cerebellum
phenotype
Finding
116
5
0.100
None
0
Aplasia/Hypoplasia of the corpus callosum
phenotype
Finding
108
8
0.100
None
0
×
CUI:
C0003578
Disease:
Apnea
Apnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
262
11
0.100
None
0
Ascites
phenotype
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
198
7
0.100
None
0
Ataxia Telangiectasia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
384
698
0.010
None
1.000
1
2008
2008
Atrial Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
384
96
0.100
None
0
Autism Spectrum Disorders
disease
Mental Disorders
Mental or Behavioral Dysfunction
1071
331
0.010
None
1.000
1
2017
2017
Barrett Esophagus
disease
Digestive System Diseases; Neoplasms
Disease or Syndrome
478
60
0.010
None
1.000
1
2004
2004