Feeding difficulties
phenotype
Finding
473
62
0.100
None
0
Mitochondrial Myopathies
group
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
121
19
0.100
None
0
Encephalopathies
group
Nervous System Diseases
Disease or Syndrome
457
64
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
Hypoglycemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
420
42
0.100
None
0
Hepatomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Finding
523
30
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
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
Fetal Distress
disease
Pathological Conditions, Signs and Symptoms
Pathologic Function
44
1
0.100
None
0
Failure to Thrive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
842
10
0.100
None
0
Hypertrophic Cardiomyopathy
disease
Cardiovascular Diseases
Disease or Syndrome
560
635
0.100
None
0
Blepharoptosis
disease
Eye Diseases
Disease or Syndrome
595
57
0.100
None
0
Ataxia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
868
68
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
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
Microcephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Congenital Abnormality
1064
27
0.100
None
0
Vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
303
23
0.100
None
0
Strabismus
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
716
89
0.100
None
0
Respiratory Insufficiency
phenotype
Respiratory Tract Diseases
Pathologic Function
315
15
0.100
None
0
Ptosis
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
607
12
0.100
None
0
Disorder of the optic nerve
group
Eye Diseases; Nervous System Diseases
Disease or Syndrome
112
2
0.100
None
0
Optic Atrophy
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
568
51
0.100
None
0
Nystagmus
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
833
95
0.100
None
0
Myopathy
group
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
634
166
0.100
None
0
Muscle hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
967
579
0.100
None
0