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PMO Precision Medicine Ontology
Last uploaded:
December 16, 2020
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| Preferred Name | Peroxisomal Disorders | |
| Synonyms |
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|
| Definitions |
An inherited metabolic disorder that involves peroxisome malfunction. |
|
| ID |
http://www.phoc.org.cn/pmo/class/PMO_00036699 |
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| Database_Cross_Reference |
RCD:X40We NDFRT:N0000003876 DO:DOID:906 NCI_NICHD:C85005 MEDCIN:275291 NCI:C85005 LCH_NW:sh90001241 ICD10CM:E71.50 ICD9CM:277.86 SNOMEDCT_US:238059005 ICD10CM:E71.5 MSH:D018901 CHV:0000027632 MEDCIN:315389
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|
| Definition |
An inherited metabolic disorder that involves peroxisome malfunction.
|
|
| label |
Peroxisomal Disorders
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|
| MCID |
MC00098971
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|
| PMOID |
PMO:00036699
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|
| prefixIRI |
pmo:PMO_00036699
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|
| prefLabel |
Peroxisomal Disorders
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|
| Synonym |
Disorder of Peroxisomal Function peroxisomal disorder (diagnosis) peroxisomal disorders Disorder of peroxisomal function (disorder) Peroxisomal Disorders [Disease/Finding] peroxisomal disorder Peroxisomal disorders peroxisomal biogenesis disorder Disord of peroxisomal function peroxisomal biogenesis disorder (diagnosis) peroxisomal disease Peroxisomal disorder, unspecified Peroxisomal Disorder PEROXISOMAL DIS Disorder of peroxisomal function Peroxisomal Function Disorder
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| Tree Number |
T9.8.4.14.11 T9.11.1.12.11
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| subClassOf |
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