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PMO Precision Medicine Ontology
Last uploaded:
December 16, 2020
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Preferred Name | Neurofibromas | |
Synonyms |
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Definitions |
The presence of multiple cutaneous neurofibromas. |
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ID |
http://www.phoc.org.cn/pmo/class/PMO_00010526 |
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Database_Cross_Reference |
ICD9CM:237.7 ICD9CM:237.70 ICPC2P:A90012 MTH:NOCODE HPO:HP:0001067 CCPSS:1014171 NCI_NICHD:C6727 MSH:D017253 MEDLINEPLUS:1387 NCI:C6727 SNM:M-9540/1 RCD:BBe1. LCH:U003188 DXP:U001284 SNMI:M-95401 LCH_NW:sh85091121 CSP:2012-7338 ICPC2P:N76001 COSTAR:U000475 SNMI:D4-01018 MDR:10029268 SNOMEDCT_US:154642000 ICD10CM:Q85.00 MEDCIN:99819 NDFRT:N0000003564 SNM:D-5425 SNOMEDCT_US:19133005 NCI_CTEP-SDC:10029268 DXP:NOCODE SNOMEDCT_US:81669005 RCDSY:BBe1. RCD:Xa99T ICD10AM:M9540/1 MDR:10029272 CHV:0000017943
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Definition |
The presence of multiple cutaneous neurofibromas.
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equivalentClass | ||
label |
Neurofibromas
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MCID |
MC00063362
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PMOID |
PMO:00010526
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prefixIRI |
pmo:PMO_00010526
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prefLabel |
Neurofibromas
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Synonym |
Syndromes, Neurofibromatosis Multiple Neurofibroma Neurofibromas neurofibromatosis (diagnosis) Neurofibromas, Multiple [M]Neurofibromatosis NOS Neurofibromatosis (morphologic abnormality) Neurofibromatoses [M]Multiple neurofibromatosis Neurofibromatosis syndrome (disorder) Neurofibromatosis syndrome Neurofibromata Multiple neurofibromatosis NEUROFIBROMA, MULTIPLE Neurofibromatosis Syndrome, Neurofibromatosis Neurofibromatoses [Disease/Finding] Neurofibromatosis (disorder) Neurofibromatosis NOS Neurofibromatosis, unspecified NF - Neurofibromatosis Clinical neurofibromatosis Neurofibromatosis, NOS Neurofibromatosis Syndromes Multiple Neurofibromas
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Tree Number |
T3.17.4.2.1.1
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subClassOf |
http://www.phoc.org.cn/pmo/class/PMO_00039335 http://www.phoc.org.cn/pmo/class/PMO_00038088 http://www.phoc.org.cn/pmo/class/PMO_00038144 http://www.phoc.org.cn/pmo/class/PMO_00038375 |
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Mapping To | Ontology | Source |
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http://purl.bioontology.org/ontology/OMIM/MTHU014989 | OMIM | LOOM |
http://purl.org/obo/owl/HP#HP_0001067 | BDO | LOOM |
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2146 | IFAR | LOOM |