ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
disease
Disease or Syndrome
18
10
0.010
None
1.000
1
2010
2010
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
disease
Disease or Syndrome
18
11
0.010
None
1.000
1
2010
2010
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
disease
Disease or Syndrome
25
7
0.010
None
1.000
1
2010
2010
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Disease or Syndrome
25
35
0.010
None
1.000
1
2010
2010
Tuberculosis, Spinal
disease
Infections; Musculoskeletal Diseases
Disease or Syndrome
29
8
0.010
None
1.000
1
2017
2017
Pneumoconiosis
disease
Respiratory Tract Diseases; Occupational Diseases
Disease or Syndrome
33
4
0.010
None
1.000
1
2017
2017
Pure Red-Cell Aplasia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
49
7
0.010
None
1.000
1
1
2011
2011
Non-Functioning Pituitary Gland Neoplasm
disease
Neoplasms; Nervous System Diseases; Endocrine System Diseases
Neoplastic Process
56
2
0.010
None
1.000
1
2019
2019
Corneal pannus
disease
Pathological Conditions, Signs and Symptoms; Eye Diseases
Disease or Syndrome
66
0.010
None
1.000
1
2019
2019
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
Tumor-Associated Vasculature
disease
Acquired Abnormality
84
0.010
None
1.000
1
2008
2008
Crohn's disease of large bowel
disease
Digestive System Diseases
Disease or Syndrome
96
1
0.010
None
1.000
1
2017
2017
Peritoneal Fibrosis
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Disease or Syndrome
104
0.020
None
1.000
2
2012
2019
Glucocorticoid Receptor Deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
104
12
0.010
None
1.000
1
2016
2016
Tactile Allodynia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
114
0.010
None
1.000
1
2018
2018
Pituitary-dependent Cushing's disease
disease
Nervous System Diseases; Endocrine System Diseases
Disease or Syndrome
115
8
0.020
None
1.000
2
2013
2016
Mitochondrial Myopathies
group
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
121
19
0.010
None
1.000
1
2011
2011
Renal interstitial fibrosis
disease
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases
Disease or Syndrome
138
0.010
None
1.000
1
2017
2017
Teratocarcinoma
disease
Neoplasms
Neoplastic Process
141
1
0.010
None
1.000
1
2004
2004
invasive cancer
phenotype
Neoplasms
Neoplastic Process
146
15
0.010
None
1.000
1
2017
2017
Hyperalgesia, Thermal
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
154
0.010
None
1.000
1
2018
2018
Keratitis
disease
Eye Diseases
Disease or Syndrome
156
10
0.010
None
1.000
1
2017
2017
Uranostaphyloschisis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
190
75
0.010
None
1.000
1
2013
2013
Autoimmune hepatitis
disease
Digestive System Diseases
Disease or Syndrome
190
22
0.010
None
1.000
1
2020
2020
×
CUI:
C0018099
Disease:
Gout
Gout
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
205
2354
0.010
None
1.000
1
2019
2019