Fetal Distress
disease
Pathological Conditions, Signs and Symptoms
Pathologic Function
44
1
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
Sensorineural Hearing Loss (disorder)
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
783
111
0.100
None
0
Ventricular Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
426
87
0.100
None
0
Hepatomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Finding
523
30
0.100
None
0
Hypertrichosis
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
92
27
0.100
None
0
Hypoglycemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
420
42
0.100
None
0
Irritable Mood
phenotype
Behavior and Behavior Mechanisms
Finding
142
1
0.100
None
0
Failure to Thrive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
842
10
0.100
None
0
Dystonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
453
97
0.100
None
0
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
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
Ataxia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
868
68
0.100
None
0
Blepharoptosis
disease
Eye Diseases
Disease or Syndrome
595
57
0.100
None
0
Peripheral Nervous System Diseases
group
Nervous System Diseases
Disease or Syndrome
549
69
0.100
None
0
Deglutition Disorders
group
Digestive System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
389
50
0.100
None
0
Diabetes Mellitus
group
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
2803
824
0.100
None
0
Dysarthria
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Mental or Behavioral Dysfunction
487
54
0.100
None
0
Nystagmus, CTCAE 5.0
phenotype
Finding
779
0.100
None
0
Lethargy
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Sign or Symptom
160
6
0.100
None
0
Leukodystrophy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
190
27
0.100
None
0
Retinitis Pigmentosa
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Disease or Syndrome
546
541
0.100
None
0
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.100
None
0
Severe intellectual disability
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
429
74
0.100
None
0
Strabismus
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
716
89
0.100
None
0