Micrognathism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
Congenital Abnormality
586
53
0.100
None
0
1
Patent ductus arteriosus
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
510
56
0.100
None
0
Diarrhea
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
632
63
0.100
None
0
Hepatosplenomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases
Sign or Symptom
127
21
0.100
None
0
1
Cyanosis
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
54
2
0.100
None
0
1
Cryptorchidism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
Congenital Abnormality
725
80
0.100
None
0
Congenital clubfoot
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
285
44
0.100
None
0
Cholestasis
disease
Digestive System Diseases
Disease or Syndrome
420
15
0.100
None
0
Ascites
phenotype
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
198
7
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
1
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
0.100
None
0
Failure to Thrive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
842
10
0.100
None
0
Fetal Distress
disease
Pathological Conditions, Signs and Symptoms
Pathologic Function
44
1
0.100
None
0
1
Macroglossia
disease
Stomatognathic Diseases
Disease or Syndrome
115
2
0.100
None
0
1
Lymphedema
disease
Hemic and Lymphatic Diseases
Pathologic Function
61
1
0.100
None
0
Microcephaly (physical finding)
phenotype
Finding
160
246
0.100
None
0
1
Hypothyroidism
disease
Endocrine System Diseases
Disease or Syndrome
613
283
0.100
None
0
1
Orbital separation excessive
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
590
77
0.100
None
0
1
Polyhydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
208
28
0.100
None
0
1
Hepatomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Finding
523
30
0.100
None
0
Heart Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
77
12
0.100
None
0
Fetal Growth Retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
1037
21
0.100
None
0
Abdomen distended
phenotype
Digestive System Diseases
Finding
103
6
0.100
None
0
Cystic liver disease
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms
Disease or Syndrome
19
0.300
None
1.000
1
2018
2018
Cystic Kidney Diseases
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
50
0.300
None
1.000
1
2018
2018