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Obsoletion status of xref update (#8508)
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* [create-pull-request] automated change

* updated xref equivalent status to match term obsoletion status in source

* fix qc check errors

* revert Orphanet xref for MONDO:0015238 to equivalentObsolete

* revert Orphanet xref for MONDO:0009971 to MONDO:equivalentObsolete

* revert Orphanet xref for MONDO:0011054 to equivalentObsolete

* revert DOID xref on MONDO:0013209 to equivalentObsolete

* revert Orphanet xref on MONDO:0015637 to equivalentObsolete

* revert Orphanet xref on MONDO:0015638 to equivalentObsolete

* revert Orphanet xref on MONDO:0015639 to equivalentObsolete

* revert Orphanet xref for MONDO:0016022 to equivalentObsolete

* revert Orphanet xref on MONDO:0018932 to equivalentObsolete

* reverted Orphanet xref on MONDO:0018981 to equivalentObsolete

* revert Orphanet xref on MONDO:0033672 to equivalentObsolete

---------

Co-authored-by: twhetzel <[email protected]>
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twhetzel and twhetzel authored Jan 5, 2025
1 parent 0a5d733 commit b1c0951
Showing 1 changed file with 26 additions and 26 deletions.
52 changes: 26 additions & 26 deletions src/ontology/mondo-edit.obo
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Expand Up @@ -32678,7 +32678,7 @@ xref: MedDRA:10016221 {source="Orphanet:99906/e", source="Orphanet:99906"}
xref: MEDGEN:8785 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:D005203 {source="Orphanet:99906/e", source="Orphanet:99906", source="DOID:14453"}
xref: NCIT:C34605 {source="MONDO:equivalentTo", source="DOID:14453"}
xref: Orphanet:99906 {source="MONDO:equivalentTo"}
xref: Orphanet:99906 {source="MONDO:equivalentObsolete"}
xref: SCTID:155581001 {source="DOID:14453"}
xref: SCTID:18690003 {source="MONDO:equivalentTo", source="DOID:14453"}
xref: SCTID:266399001 {source="DOID:14453"}
Expand Down Expand Up @@ -110423,7 +110423,7 @@ xref: MedDRA:10004941 {source="Orphanet:99908/e", source="Orphanet:99908"}
xref: MEDGEN:586 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:D001716 {source="Orphanet:99908/e", source="MONDO:equivalentTo", source="EFO:0007170", source="DOID:13891", source="Orphanet:99908"}
xref: NCIT:C34425 {source="MONDO:equivalentTo", source="DOID:13891"}
xref: Orphanet:99908 {source="MONDO:equivalentTo"}
xref: Orphanet:99908 {source="MONDO:equivalentObsolete"}
xref: SCTID:195987000 {source="DOID:13891"}
xref: SCTID:69339004 {source="MONDO:equivalentTo", source="DOID:13891"}
xref: UMLS:C0005592 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:586"}
Expand Down Expand Up @@ -140991,7 +140991,7 @@ synonym: "anemia due to adenosine triphosphatase deficiency" RELATED [GARD:00005
xref: GARD:548 {source="MONDO:GARD"}
xref: MEDGEN:350115 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:C566311 {source="MONDO:equivalentTo"}
xref: OMIM:102800 {source="MONDO:equivalentTo"}
xref: OMIM:102800 {source="MONDO:equivalentObsolete"}
xref: Orphanet:1044 {source="MONDO:equivalentObsolete", source="OMIM:102800"}
xref: SCTID:725057008 {source="MONDO:equivalentTo"}
xref: UMLS:C1863225 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:350115"}
Expand Down Expand Up @@ -158045,7 +158045,7 @@ xref: GARD:16724 {source="MONDO:GARD"}
xref: ICD10CM:E78.4 {source="Orphanet:79506/attributed", source="Orphanet:79506/ntbt", source="Orphanet:79506"}
xref: MEDGEN:840020 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: OMIM:143470 {source="Orphanet:79506", source="MONDO:equivalentTo", source="Orphanet:79506/e"}
xref: Orphanet:79506 {source="OMIM:143470", source="MONDO:equivalentTo"}
xref: Orphanet:79506 {source="MONDO:equivalentObsolete", source="OMIM:143470"}
xref: SCTID:15771000119109 {source="MONDO:equivalentTo"}
xref: UMLS:C3875011 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:840020"}
is_a: MONDO:0015903 {source="Orphanet:79506"} ! hyperalphalipoproteinemia
Expand Down Expand Up @@ -174638,7 +174638,7 @@ xref: MESH:D008949 {source="MONDO:equivalentTo", source="DOID:452"}
xref: NCIT:C35691 {source="DOID:452"}
xref: NCIT:C8602 {source="MONDO:equivalentTo", source="DOID:452"}
xref: OMIM:181030 {source="MONDO:equivalentTo", source="Orphanet:454821", source="DOID:452", source="Orphanet:454821/e"}
xref: Orphanet:454821 {source="MONDO:equivalentTo"}
xref: Orphanet:454821 {source="MONDO:equivalentObsolete"}
xref: SCTID:447888006 {source="MONDO:equivalentTo"}
xref: SCTID:8360001 {source="DOID:452"}
xref: UMLS:C1519176 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:275400"}
Expand Down Expand Up @@ -218560,7 +218560,7 @@ xref: MESH:C566881 {source="MONDO:equivalentTo"}
xref: MESH:D006819 {source="DOID:12716", source="EFO:1000644"}
xref: NORD:1659 {source="MONDO:NORD"}
xref: OMIM:267450 {source="MONDO:equivalentTo", source="Orphanet:70587", source="DOID:12716", source="EFO:1000644", source="Orphanet:70587/e"}
xref: Orphanet:70587 {source="OMIM:267450", source="MONDO:equivalentTo"}
xref: Orphanet:70587 {source="OMIM:267450", source="MONDO:equivalentObsolete"}
xref: UMLS:C1968593 {source="MEDGEN:368840", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0002254 {source="NCIT:C27560"} ! syndromic disease
is_a: MONDO:0017015 {source="Orphanet:70587"} ! primary interstitial lung disease specific to childhood
Expand Down Expand Up @@ -241038,7 +241038,7 @@ subset: obsoletion_candidate
synonym: "XH antigen" EXACT []
xref: MEDGEN:854528 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:C009691 {source="MONDO:equivalentTo"}
xref: OMIM:314800 {source="MONDO:equivalentTo"}
xref: OMIM:314800 {source="MONDO:equivalentObsolete"}
xref: UMLS:C3887689 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:854528"}
is_a: MONDO:0003847 {source="https://orcid.org/0000-0001-5208-3432"} ! hereditary disease
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8409" xsd:anyURI
Expand Down Expand Up @@ -246991,7 +246991,7 @@ synonym: "telangiectasia, hereditary hemorrhagic, type 3" RELATED [MONDO:Lexical
xref: GARD:9902 {source="MONDO:GARD"}
xref: MEDGEN:371403 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:C537140 {source="MONDO:equivalentTo"}
xref: OMIM:601101 {source="GARD:0009902", source="MONDO:equivalentTo"}
xref: OMIM:601101 {source="GARD:0009902", source="MONDO:equivalentObsolete"}
xref: Orphanet:774 {source="GARD:0009902", source="OMIM:601101"}
xref: UMLS:C1832774 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:371403"}
is_a: MONDO:0019180 {source="DC-OMIM:601101", source="MESH:C537140", source="OMIM:601101"} ! hereditary hemorrhagic telangiectasia
Expand Down Expand Up @@ -248498,7 +248498,7 @@ xref: ICD10CM:Q73.0 {source="Orphanet:1027", source="Orphanet:1027/attributed",
xref: MEDGEN:321955 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:C563338 {source="MONDO:equivalentTo"}
xref: OMIM:601360 {source="MONDO:equivalentTo", source="Orphanet:1027", source="Orphanet:1027/e"}
xref: Orphanet:1027 {source="MONDO:equivalentTo", source="OMIM:601360"}
xref: Orphanet:1027 {source="MONDO:equivalentObsolete", source="OMIM:601360"}
xref: SCTID:726735000 {source="MONDO:equivalentTo"}
xref: UMLS:C1832432 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:321955"}
is_a: MONDO:0006025 {source="MONDO:Redundant"} ! autosomal recessive disease
Expand Down Expand Up @@ -292796,7 +292796,7 @@ xref: MESH:C567379 {source="MONDO:equivalentTo"}
xref: NANDO:1200362 {source="MONDO:NANDO", source="https://orcid.org/0000-0003-0011-764X", source="https://orcid.org/0000-0002-0170-9172"}
xref: NANDO:2200763 {source="MONDO:NANDO", source="https://orcid.org/0000-0003-0011-764X", source="https://orcid.org/0000-0002-0170-9172"}
xref: OMIM:612260 {source="Orphanet:183713/e", source="MONDO:equivalentTo", source="Orphanet:183713"}
xref: Orphanet:183713 {source="MONDO:equivalentTo", source="OMIM:612260"}
xref: Orphanet:183713 {source="MONDO:equivalentObsolete", source="OMIM:612260"}
xref: UMLS:C2677092 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:383023"}
is_a: MONDO:0021094 {source="OMIM:612260", source="https://orcid.org/0000-0001-5208-3432"} ! immunodeficiency disease
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/hgnc/7562 {source="MONDO:mim2gene_medgen", source="OMIM:612260"} ! MYD88
Expand Down Expand Up @@ -302116,7 +302116,7 @@ synonym: "non-alcoholic fatty liver" EXACT [DOID:0080546, MONDO:0007026]
synonym: "non-alcoholic fatty liver disease" EXACT [DOID:0080208, NCIT:C84444]
synonym: "nonalcoholic fatty liver disease" EXACT [DOID:0080208, NCIT:C84444]
xref: DOID:0080208 {source="MONDO:equivalentTo", source="MONDO:preferredExternal"}
xref: DOID:0080546 {source="MONDO:equivalentTo"}
xref: DOID:0080546 {source="MONDO:equivalentObsolete"}
xref: EFO:0003095 {source="MONDO:equivalentTo", source="MONDO:EFO"}
xref: ICD9:571.8 {source="MONDO:relatedTo", source="MONDO:i2s"}
xref: MedDRA:10029530 {source="EFO:1001248"}
Expand Down Expand Up @@ -351654,7 +351654,7 @@ synonym: "congenital absence of nose and anterior nasopharynx" RELATED [GARD:000
xref: GARD:8755 {source="MONDO:GARD"}
xref: ICD10CM:Q87.0 {source="Orphanet:1135/attributed", source="Orphanet:1135/ntbt", source="Orphanet:1135"}
xref: NORD:1909 {source="MONDO:NORD"}
xref: Orphanet:1135 {source="GARD:0008755", source="MONDO:equivalentTo"}
xref: Orphanet:1135 {source="GARD:0008755", source="MONDO:equivalentObsolete"}
is_a: MONDO:0015161 {source="Orphanet:1135"} ! multiple congenital anomalies/dysmorphic syndrome without intellectual disability
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7813" xsd:anyURI
property_value: IAO:0006012 "2025-02-01" xsd:string
Expand Down Expand Up @@ -360269,7 +360269,7 @@ subset: rare
xref: GARD:20071 {source="MONDO:GARD"}
xref: ICD10CM:G40.4 {source="Orphanet:166295/attributed", source="Orphanet:166295/ntbt", source="Orphanet:166295"}
xref: MEDGEN:1843116 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:166295 {source="MONDO:equivalentTo"}
xref: Orphanet:166295 {source="MONDO:equivalentObsolete"}
xref: UMLS:C5680425 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:1843116"}
is_a: MONDO:0015642 {source="Orphanet:166295"} ! benign partial infantile seizures

Expand All @@ -360284,7 +360284,7 @@ xref: GARD:20072 {source="MONDO:GARD"}
xref: ICD10CM:G40.2 {source="Orphanet:166299", source="Orphanet:166299/attributed", source="Orphanet:166299/ntbt"}
xref: icd11.foundation:147618459 {source="MONDO:equivalentTo"}
xref: MEDGEN:1654146 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:166299 {source="MONDO:equivalentTo"}
xref: Orphanet:166299 {source="MONDO:equivalentObsolete"}
xref: UMLS:C4749347 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:1654146"}
is_a: MONDO:0015637 {source="Orphanet:166299"} ! benign non-familial infantile seizures

Expand All @@ -360299,7 +360299,7 @@ xref: GARD:20073 {source="MONDO:GARD"}
xref: ICD10CM:G40.1 {source="Orphanet:166302", source="Orphanet:166302/attributed", source="Orphanet:166302/ntbt"}
xref: icd11.foundation:413225821 {source="MONDO:equivalentTo"}
xref: MEDGEN:1656339 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:166302 {source="MONDO:equivalentTo"}
xref: Orphanet:166302 {source="MONDO:equivalentObsolete"}
xref: UMLS:C4749728 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:1656339"}
is_a: MONDO:0015637 {source="Orphanet:166302"} ! benign non-familial infantile seizures

Expand Down Expand Up @@ -366858,7 +366858,7 @@ xref: GARD:920 {source="MONDO:obsoleteEquivalent", source="MONDO:GARD"}
xref: ICD10CM:Q78.4 {source="Orphanet:1844/inclusion", source="Orphanet:1844", source="Orphanet:1844/ntbt"}
xref: icd11.foundation:2054115498 {source="MONDO:obsoleteEquivalent"}
xref: MEDGEN:929662 {source="MONDO:obsoleteEquivalent", source="MONDO:MEDGEN"}
xref: Orphanet:1844 {source="MONDO:obsoleteEquivalent"}
xref: Orphanet:1844 {source="MONDO:obsoleteEquivalentObsolete"}
xref: SCTID:720566004 {source="MONDO:obsoleteEquivalent"}
xref: UMLS:C4303993 {source="MONDO:obsoleteEquivalent", source="MEDGEN:929662", source="MONDO:MEDGEN"}
property_value: IAO:0000231 OMO:0001000 {source="MONDO:excludeHistoricalDisease"}
Expand Down Expand Up @@ -367834,7 +367834,7 @@ xref: MEDGEN:124373 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:D004831 {source="DOID:308"}
xref: NANDO:1200594 {source="MONDO:NANDO", source="https://orcid.org/0000-0003-0011-764X", source="https://orcid.org/0000-0002-0170-9172"}
xref: NCIT:C116593 {source="MONDO:equivalentTo"}
xref: Orphanet:1935 {source="MONDO:equivalentTo"}
xref: Orphanet:1935 {source="MONDO:equivalentObsolete"}
xref: SCTID:192847001 {source="DOID:308"}
xref: SCTID:192992007 {source="DOID:308"}
xref: SCTID:37356005 {source="DOID:308"}
Expand Down Expand Up @@ -392075,7 +392075,7 @@ subset: rare
synonym: "Heide syndrome" EXACT [Orphanet:2787]
xref: GARD:18778 {source="MONDO:GARD"}
xref: MEDGEN:899606 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:2787 {source="MONDO:equivalentTo"}
xref: Orphanet:2787 {source="MONDO:equivalentObsolete"}
xref: SCTID:716189005 {source="MONDO:equivalentTo"}
xref: UMLS:C4274786 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:899606"}
is_a: MONDO:0002254 {source="https://orcid.org/0000-0001-5208-3432"} ! syndromic disease
Expand Down Expand Up @@ -412668,7 +412668,7 @@ xref: GARD:18823 {source="MONDO:GARD"}
xref: ICD10CM:I72.0 {source="Orphanet:36382", source="Orphanet:36382/attributed", source="Orphanet:36382/ntbt"}
xref: ICD10CM:I72.5 {source="Orphanet:36382", source="Orphanet:36382/attributed", source="Orphanet:36382/ntbt"}
xref: MEDGEN:1659372 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:36382 {source="MONDO:equivalentTo"}
xref: Orphanet:36382 {source="MONDO:equivalentObsolete"}
xref: UMLS:C4755308 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:1659372"}
is_a: MONDO:0006061 {source="https://orcid.org/0000-0001-5208-3432"} ! cervical artery dissection
intersection_of: MONDO:0006061 ! cervical artery dissection
Expand Down Expand Up @@ -419873,7 +419873,7 @@ name: obsolete intellectual disability-expressive aphasia-facial dysmorphism syn
subset: otar {source="MONDO:OTAR"}
synonym: "intellectual disability-loss of expressive language-facial dysmorphism syndrome" EXACT []
xref: ICD10CM:Q87.0 {source="Orphanet:436151", source="Orphanet:436151/attributed", source="Orphanet:436151/ntbt"}
xref: Orphanet:436151 {source="MONDO:obsoleteEquivalent"}
xref: Orphanet:436151 {source="MONDO:obsoleteEquivalentObsolete"}
relationship: excluded_subClassOf MONDO:0000508 {source="Orphanet:436151", source="https://orcid.org/0000-0001-5208-3432"} ! syndromic intellectual disability
property_value: IAO:0000231 OMO:0001000 {source="MONDO:excludeGrouping"}
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/5114" xsd:anyURI
Expand Down Expand Up @@ -427592,7 +427592,7 @@ xref: GARD:18852 {source="MONDO:GARD"}
xref: ICD10CM:I42.8 {source="Orphanet:57777", source="Orphanet:57777/ntbt"}
xref: icd11.foundation:1268082489 {source="MONDO:equivalentTo"}
xref: MEDGEN:1391593 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:57777 {source="MONDO:equivalentTo"}
xref: Orphanet:57777 {source="MONDO:equivalentObsolete"}
xref: SCTID:725416005 {source="MONDO:equivalentTo"}
xref: UMLS:C4511053 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:1391593"}
is_a: MONDO:0016330 {source="Orphanet:57777"} ! non-familial hypertrophic cardiomyopathy
Expand Down Expand Up @@ -429053,7 +429053,7 @@ xref: GARD:18860 {source="MONDO:GARD"}
xref: ICD10CM:G40.4 {source="Orphanet:64545/ntbt", source="Orphanet:64545"}
xref: icd11.foundation:1131336245 {source="MONDO:equivalentTo"}
xref: MEDGEN:140738 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:64545 {source="MONDO:equivalentTo"}
xref: Orphanet:64545 {source="MONDO:equivalentObsolete"}
xref: UMLS:C0393693 {source="MEDGEN:140738", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0020070 {source="Orphanet:64545"} ! neonatal epilepsy syndrome
relationship: has_characteristic HP:0003623 {source="Orphanet:64545"} ! Neonatal onset
Expand Down Expand Up @@ -461600,7 +461600,7 @@ xref: GARD:19703 {source="MONDO:GARD"}
xref: ICD10CM:J67.8 {source="Orphanet:99907/ntbt", source="Orphanet:99907"}
xref: icd11.foundation:1985023223 {source="MONDO:equivalentTo"}
xref: MEDGEN:1387737 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:99907 {source="MONDO:equivalentTo"}
xref: Orphanet:99907 {source="MONDO:equivalentObsolete"}
xref: SCTID:725415009 {source="MONDO:equivalentTo"}
xref: UMLS:C4511048 {source="MEDGEN:1387737", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0017853 {source="Orphanet:99907"} ! hypersensitivity pneumonitis
Expand All @@ -461617,7 +461617,7 @@ replaced_by: MONDO:0005668
id: MONDO:0020537
name: obsolete occupational allergic alveolitis
def: "OBSOLETE. Occupational allergic alveolitis designates a hypersensitivity pneumonitis resulting from the inhalation of an antigen to which an individual has been previously sensitized in his/her occupational environment. Symptoms vary depending on the antigen and the form (acute, subacute, chronic) of the disease. They may be cough, dyspnea, chills, fever, weight loss, loss of appetite and general malaise" [Orphanet:99909]
xref: Orphanet:99909 {source="MONDO:obsoleteEquivalent"}
xref: Orphanet:99909 {source="MONDO:obsoleteEquivalentObsolete"}
property_value: IAO:0000231 OMO:0001000 {source="MONDO:excludeGrouping"}
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/5114" xsd:anyURI
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/6693" xsd:anyURI
Expand Down Expand Up @@ -513710,7 +513710,7 @@ subset: gard_rare {source="GARD:18842", source="MONDO:GARD"}
subset: rare
xref: GARD:18842 {source="MONDO:GARD"}
xref: MEDGEN:928219 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: Orphanet:50817 {source="MONDO:equivalentTo"}
xref: Orphanet:50817 {source="MONDO:equivalentObsolete"}
xref: UMLS:C4302550 {source="MEDGEN:928219", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0000001 {source="Orphanet:50817"} ! disease
is_a: MONDO:0002254 {source="https://orcid.org/0000-0002-4142-7153"} ! syndromic disease
Expand Down Expand Up @@ -528508,7 +528508,7 @@ xref: EFO:1001967 {source="MONDO:equivalentTo", source="MONDO:EFO"}
xref: GARD:17929 {source="MONDO:GARD"}
xref: MEDGEN:83545 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C7991 {source="MONDO:equivalentTo"}
xref: Orphanet:500481 {source="MONDO:equivalentTo"}
xref: Orphanet:500481 {source="MONDO:equivalentObsolete"}
xref: UMLS:C0279697 {source="MEDGEN:83545", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0000521 {source="MONDO:Redundant", source="NCIT:C7991"} ! salivary gland carcinoma
is_a: MONDO:0010150 {source="NCIT:C7991"} ! head and neck squamous cell carcinoma
Expand Down

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