MITOCHONDRIAL COMPLEX I DEFICIENCY
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
40
31
0.500
None
1.000
3
2008
2016
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
disease
Disease or Syndrome
51
4
0.010
None
1.000
1
2008
2008
Blepharoptosis
disease
Eye Diseases
Disease or Syndrome
595
57
0.100
None
0
Hypertrophic Cardiomyopathy
disease
Cardiovascular Diseases
Disease or Syndrome
560
635
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
Sensorineural Hearing Loss (disorder)
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
783
111
0.100
None
0
Hypoglycemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
420
42
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
Nystagmus
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
833
95
0.100
None
0
Optic Atrophy
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
568
51
0.100
None
0
Ptosis
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
607
12
0.100
None
0
Strabismus
disease
Eye Diseases; Nervous System Diseases
Disease or Syndrome
716
89
0.100
None
0
Cerebral atrophy
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
454
44
0.100
None
0
Global developmental delay
disease
Mental or Behavioral Dysfunction
1825
553
0.100
None
0
Abnormal mitochondria in muscle tissue
disease
Anatomical Abnormality
39
2
0.100
None
0
Brain atrophy
disease
Nervous System Diseases
Disease or Syndrome
182
46
0.100
None
0
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14
disease
Disease or Syndrome
1
1
0.400
strong
0
1
Body Height
phenotype
Organism Attribute
1903
3972
0.100
None
1.000
1
1
2019
2019
Lactic acidemia
phenotype
Disease or Syndrome
12
0.010
None
1.000
1
2008
2008
Acidosis, Lactic
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
209
21
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
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