Fistula of genitourinary tract
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Anatomical Abnormality
11
0.100
None
0
Short stature
phenotype
Finding
1127
292
0.100
None
0
2
Abnormality of cardiovascular system morphology
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
198
13
0.100
None
0
Abnormality of female internal genitalia
disease
Anatomical Abnormality
31
0.100
None
0
Congenital Epicanthus
disease
Congenital Abnormality
417
30
0.100
None
0
Abnormal sacrum morphology
disease
Anatomical Abnormality
17
0.100
None
0
Non-midline cleft lip
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Congenital Abnormality
16
0.100
None
0
Multicystic Dysplastic Kidney
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
121
11
0.100
None
0
Renal dysplasia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Congenital Abnormality
95
3
0.100
None
0
Depressed nasal ridge
phenotype
Finding
117
1
0.100
None
0
Fetal polyuria
phenotype
Finding
10
0.100
None
0
Inner ear malformation
phenotype
Finding
1
2
0.100
None
0
2
Uterine Anomalies
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Congenital Abnormality
35
1
0.100
None
0
Cleft Palate
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
Congenital Abnormality
611
158
0.100
None
0
Orbital separation excessive
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
590
77
0.100
None
0
Sirenomelia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
11
0.100
None
0
Tracheoesophageal Fistula
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases
Anatomical Abnormality
80
0.100
None
0
Oligohydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
129
21
0.100
None
0
Horseshoe Kidney
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Congenital Abnormality
51
3
0.100
None
0
Renal Cell Dysplasia
disease
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
81
3
0.100
None
0
Low set ears
disease
Congenital Abnormality
489
64
0.100
None
0
Congenital hypoplasia of lung
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Congenital Abnormality
175
6
0.100
None
0
Abnormality of the intestine
phenotype
Finding
19
0.100
None
0
Nonketotic hypoglycemia
phenotype
Nutritional and Metabolic Diseases
Finding
11
0.100
None
0
×
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
2017
2017