loading...| Preferred Name |
Tyrosinemias |
|
| Synonyms |
|
|
| Definitions |
An amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine. |
|
| ID |
http://www.phoc.org.cn/pmo/class/PMO_00038504 |
|
| Database_Cross_Reference |
LNC:LP56753-4 MTH:NOCODE MEDCIN:33609 CHV:0000026314 SNOMEDCT_US:190694001 MSH:D020176 CSP:1849-1291 NDFRT:N0000004017 LNC:MTHU021584 NCI:C98640 MDR:10063443 OMIM:MTHU037988 ICD10CM:E70.21 RCDAE:C3026 MDR:10063446 DO:DOID:9275 SNM:D-1620 RCD:C3026 |
|
| Definition |
An amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine. |
|
| label |
Tyrosinemias |
|
| MCID |
MC00092778 |
|
| PMOID |
PMO:00038504 |
|
| prefixIRI |
pmo:PMO_00038504 |
|
| prefLabel |
Tyrosinemias |
|
| Synonym |
Tyrosinaemia Hereditary Tyrosinemia Tyrosinemia (disorder) tyrosinaemia Tyrosinemias, Hereditary Tyrosinemias [Disease/Finding] Hypertyrosinemia Tyrosinemia, Hereditary hereditary tyrosinemia tyrosinemia Hereditary Tyrosinemias Tyrosinemia tyrosinemia (diagnosis) |
|
| Tree Number |
T9.11.1.12.6.2 T9.8.4.14.6.2 T9.11.1.6.2.10 T9.8.4.14.8.10 T9.21.15.5.17.2.10 T9.11.1.12.8.10 |
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| subClassOf |