Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dihydrolipoamide dehydrogenase deficiency |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile myopathy, encephalopathy, lactic acidosis, stroke (disorder) |
Is a |
False |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pyruvate dehydrogenase complex deficiency |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Infantile encephalopathy AND lactic acidosis (disorder) |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pyruvate carboxylase deficiency (disorder) |
Is a |
False |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Metabolic acidosis due to grain overload (disorder) |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis (disorder) |
Associated with |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
D-lactic acidosis |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare metabolic myopathy presenting during childhood, and characterized clinically by growth failure, severe muscle weakness, and moderate sensorineural deafness and biochemically by metabolic acidosis, elevated serum pyruvate concentration, hyperalaninemia and hyperalaninuria. There have been no further descriptions in the literature since 1973. |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lactic acidosis with diabetes mellitus |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder) |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome |
Is a |
True |
Lactic acidosis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|