| General Information | |||
|---|---|---|---|
| Term | tyrosinemia | ID (Ontology) | DOID:9275 (Human Disease) |
| Definition | An amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine. | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
inherited metabolic disorder |__amino acid metabolic disorder |__tyrosinemia 4 rec. |__tyrosinemia type I 1 rec. |__tyrosinemia type II 1 rec. |__tyrosinemia type III 2 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | amino acid metabolic disorder | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICD10CM:E70.21 SNOMEDCT_US_2023_03_01:190694001 UMLS_CUI:C0268483 |
|||