Fibrosis
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
184
0.010
None
1.000
1
2003
2003
Senior-Loken Syndrome 3
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases
Disease or Syndrome
4
0.010
None
1.000
1
2002
2002
Jaundice, Obstructive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
66
0.010
None
1.000
1
2018
2018
Liver diseases
group
Digestive System Diseases
Disease or Syndrome
1019
100
0.010
None
1.000
1
2018
2018
Hydrocephalus, Normal Pressure
disease
Nervous System Diseases
Disease or Syndrome
44
6
0.010
None
1.000
1
2000
2000
Retinal Diseases
group
Eye Diseases
Disease or Syndrome
714
56
0.010
None
1.000
1
2002
2002
Retinitis Pigmentosa
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Disease or Syndrome
546
541
0.010
None
1.000
1
2008
2008
Nephronophthisis 1
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
18
6
0.010
None
1.000
1
2002
2002
Congenital heart disease
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
267
80
0.010
None
1.000
1
1
2016
2016
Streptococcal lymphadenitis of swine
disease
Infections; Hemic and Lymphatic Diseases
Disease or Syndrome
13
1
0.010
None
1.000
1
2002
2002
Deformity
group
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Anatomical Abnormality
350
26
0.010
None
1.000
1
2013
2013
Medullary cystic disease
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
9
0.010
None
1.000
1
2002
2002
Sjogren-Larsson Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
20
28
0.010
None
1.000
1
2002
2002
Congenital neurologic anomalies
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
84
4
0.010
None
1.000
1
2013
2013
×
CUI:
C1968949
Disease:
Cakut
Cakut
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
72
8
0.010
None
1.000
1
2008
2008
Carcinogenesis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6243
355
0.010
None
1.000
1
2019
2019
Cystic Kidney Diseases
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
50
0.020
None
1.000
2
2009
2010
Congenital cystic kidney disease
disease
Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome; Congenital Abnormality
31
0.020
None
1.000
2
2009
2010
Congenital Abnormality
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
1098
73
0.020
None
1.000
2
2009
2013
Medullary cystic kidney disease 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
5
0.020
None
1.000
2
2000
2001
Kidney Failure, Chronic
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
827
425
0.020
None
1.000
2
2001
2009
Cystic kidney
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
89
1
0.030
None
1.000
3
2001
2010
Finding of Mean Corpuscular Hemoglobin
phenotype
Finding
653
1206
0.100
None
1.000
1
1
2016
2016
Tonometry
phenotype
Diagnostic Procedure
206
573
0.100
None
1.000
1
1
2018
2018
Mean Corpuscular Volume (result)
phenotype
Laboratory or Test Result
269
549
0.100
None
1.000
1
1
2016
2016