Abnormality of dental enamel
group
Anatomical Abnormality
96
4
0.100
None
0
Abnormality of pelvic girdle bone morphology
disease
Anatomical Abnormality
55
5
0.100
None
0
Abnormality of the metaphysis
disease
Anatomical Abnormality
97
0.100
None
0
Abnormality of the skeletal system
disease
Anatomical Abnormality
148
18
0.010
None
1.000
1
2002
2002
Absence of sensation
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
111
5
0.010
None
1.000
1
2020
2020
Adult Rickets
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
47
0.160
None
1.000
6
1989
2019
Aggressive behavior
phenotype
Behavior and Behavior Mechanisms
Individual Behavior
176
22
0.100
None
1.000
1
1
2014
2014
Alcohol problem
phenotype
Mental or Behavioral Dysfunction
23
5
0.010
None
1.000
1
2009
2009
Alcoholic Intoxication, Chronic
disease
Chemically-Induced Disorders; Mental Disorders
Mental or Behavioral Dysfunction
577
441
0.010
None
1.000
1
2009
2009
Alkaline phosphatase raised
phenotype
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Finding
55
0.100
None
0
×
CUI:
C0002957
Disease:
Anger
Anger
phenotype
Behavior and Behavior Mechanisms
Mental Process
4
4
0.100
None
1.000
1
1
2014
2014
Anorgasmia
disease
Mental or Behavioral Dysfunction
1
0.010
None
1.000
1
2018
2018
Arnold-Chiari Malformation, Type I
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
41
1
0.010
None
1.000
1
2019
2019
Arthralgia
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Sign or Symptom
248
27
0.100
None
0
Arthritis, Psoriatic
disease
Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome
450
89
0.010
None
1.000
1
2015
2015
Asthma
disease
Respiratory Tract Diseases; Immune System Diseases
Disease or Syndrome
2096
1536
0.010
None
1.000
1
2019
2019
Autosomal dominant hypophosphatemic rickets
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
11
4
0.020
None
1.000
2
2001
2013
Autosomal recessive hypophosphatemic vitamin D refractory rickets
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
11
2
0.020
None
1.000
2
2013
2014
Axial myopia
disease
Eye Diseases
Disease or Syndrome
5
0.010
None
1.000
1
2019
2019
Bone Diseases, Developmental
group
Musculoskeletal Diseases
Disease or Syndrome
82
2
0.010
None
1.000
1
2015
2015
Bone pain
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Sign or Symptom
139
0.100
None
0
Bone Pain, CTCAE 3.0
phenotype
Finding
67
0.100
None
0
Bone Pain, CTCAE 5.0
phenotype
Finding
67
0.100
None
0
Cataract
disease
Eye Diseases
Acquired Abnormality
878
124
0.010
None
1.000
1
2019
2019
Central neuropathic pain
disease
Disease or Syndrome
9
0.010
None
1.000
1
2017
2017