ATP5F1D, ATP synthase F1 subunit delta, 513

N. diseases: 69; N. variants: 2
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
group Nutritional and Metabolic Diseases Disease or Syndrome 945 50 0.010 None 1.000 1 2018 2018
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
disease Neoplasms Neoplastic Process 2438 563 0.010 None 1.000 1 2002 2002
Oxidative Phosphorylation Deficiencies
disease Nutritional and Metabolic Diseases Disease or Syndrome 18 1 0.010 None 1.000 1 1 2018 2018
CUI: C4025860
Disease: Hearing abnormality
Hearing abnormality
disease Finding 24 5 0.100 None 1.000 1 1 2018 2018
CUI: C1839437
Disease: Chronic lactic acidosis
Chronic lactic acidosis
phenotype Nutritional and Metabolic Diseases Finding 4 3 0.100 None 1.000 1 1 2018 2018
CUI: C1837142
Disease: Poor suck
Poor suck
phenotype Finding 103 31 0.100 None 1.000 1 1 2018 2018
CUI: C1836940
Disease: Thickened nuchal skin fold
Thickened nuchal skin fold
phenotype Finding 58 4 0.100 None 1.000 1 1 2018 2018
CUI: C0575802
Disease: Small hand
Small hand
phenotype Finding 108 31 0.100 None 1.000 1 1 2018 2018
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding 11 54 0.100 None 1.000 1 1 2018 2018
CUI: C0476369
Disease: Echocardiogram abnormal
Echocardiogram abnormal
phenotype Finding 3 1 0.100 None 1.000 1 1 2018 2018
CUI: C0349588
Disease: Short stature
Short stature
phenotype Finding 1127 292 0.100 None 1.000 1 1 2018 2018
CUI: C0265985
Disease: Mongolian Spot
Mongolian Spot
disease Neoplasms Neoplastic Process 5 3 0.100 None 1.000 1 1 2018 2018
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 237 21 0.100 None 1.000 1 1 2018 2018
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
phenotype Finding 59 5 0.100 None 1.000 1 1 2018 2018
CUI: C1843108
Disease: Short palm
Short palm
phenotype Finding 110 13 0.100 None 1.000 1 1 2018 2018
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile
phenotype Finding 22 27 0.100 None 1.000 1 1 2018 2018
CUI: C4025790
Disease: Specific learning disability
Specific learning disability
disease Mental or Behavioral Dysfunction 165 13 0.100 None 1.000 1 1 2018 2018
CUI: C4023343
Disease: Nasogastric tube feeding in infancy
Nasogastric tube feeding in infancy
phenotype Finding 12 9 0.100 None 1.000 1 1 2018 2018
Decreased activity of mitochondrial ATP synthase complex
phenotype Finding 3 1 0.100 None 1.000 1 1 2018 2018
Abnormality of the subarachnoid space
phenotype Anatomical Abnormality 3 4 0.100 None 1.000 1 1 2018 2018
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
phenotype Finding 305 22 0.100 None 1.000 1 1 2018 2018
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders Disease or Syndrome 166 122 0.100 None 1.000 1 1 2018 2018
CUI: C1859516
Disease: Episodic metabolic acidosis
Episodic metabolic acidosis
phenotype Nutritional and Metabolic Diseases Finding 5 3 0.100 None 1.000 1 1 2018 2018
CUI: C1859506
Disease: Acute hyperammonemia
Acute hyperammonemia
phenotype Pathological Conditions, Signs and Symptoms Finding 5 1 0.100 None 1.000 1 1 2018 2018
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 955 164 0.100 None 1.000 1 1 2018 2018