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add NCIT x-refs
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addresses #8567
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@katiermullen
katiermullen committed Jan 15, 2025
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112 changes: 62 additions & 50 deletions src/ontology/mondo-edit.obo
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Expand Up @@ -25523,6 +25523,7 @@ synonym: "malignant tumour of the lacrimal duct" EXACT OMO:0003005 []
xref: DOID:12756 {source="MONDO:equivalentTo"}
xref: ICD9:190.7 {source="DOID:12756", source="MONDO:equivalentTo", source="MONDO:i2s"}
xref: MEDGEN:57795 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C175319 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C3567 {source="DOID:12756", source="MONDO:equivalentTo"}
xref: SCTID:188274004 {source="DOID:12756", source="MONDO:equivalentTo"}
xref: SCTID:188275003 {source="DOID:12756"}
Expand Down Expand Up @@ -75148,6 +75149,7 @@ synonym: "intramuscular lipoma" EXACT [DOID:7014]
synonym: "intramuscular lipoma (morphologic abnormality)" EXACT []
xref: DOID:7014 {source="MONDO:equivalentTo"}
xref: MEDGEN:90788 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C7450 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C7450 {source="DOID:7014"}
xref: NCIT:C7451 {source="MONDO:equivalentTo", source="DOID:7014"}
xref: SCTID:24045002 {source="DOID:7014"}
Expand Down Expand Up @@ -77019,6 +77021,7 @@ xref: ICD9:223.89 {source="MONDO:relatedTo", source="MONDO:i2s"}
xref: ICD9:223.9 {source="MONDO:equivalentTo", source="MONDO:i2s"}
xref: MEDGEN:146348 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:D014571 {source="DOID:731", source="MONDO:equivalentTo"}
xref: NCIT:C192667 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C3431 {source="DOID:731"}
xref: NCIT:C4893 {source="MONDO:equivalentTo"}
xref: SCTID:126879004 {source="DOID:731"}
Expand Down Expand Up @@ -83456,6 +83459,7 @@ synonym: "uterine corpus soft tissue neoplasm" EXACT []
xref: DOID:8302 {source="MONDO:equivalentTo"}
xref: MEDGEN:269077 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C40178 {source="DOID:8302", source="MONDO:equivalentTo"}
xref: NCIT:C40179 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: UMLS:C1513364 {source="MEDGEN:269077", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0006424 {source="MONDO:Redundant", source="NCIT:C40178/inferred", source="NCIT:C40179"} ! soft tissue neoplasm
is_a: MONDO:0021254 {source="MONDO:Redundant", source="NCIT:C40178/inferred", source="NCIT:C40179"} ! corpus uteri neoplasm
Expand Down Expand Up @@ -88098,8 +88102,8 @@ name: submandibular gland cancer
def: "A malignant neoplasm involving the submandibular gland." [https://orcid.org/0000-0002-6601-2165]
subset: otar {source="MONDO:OTAR"}
synonym: "cancer of submandibular gland" EXACT [MONDO:patterns/cancer]
synonym: "carcinoma of submandibular gland" EXACT [NCIT:C8396]
synonym: "carcinoma of the submandibular gland" EXACT [NCIT:C8396]
synonym: "carcinoma of submandibular gland" NARROW [https://orcid.org/0000-0002-5002-8648, NCIT:C8396]
synonym: "carcinoma of the submandibular gland" NARROW [NCIT:C8396] {NARROW="https://orcid.org/0000-0002-5002-8648"}
synonym: "malignant neoplasm of submandibular gland" EXACT [MONDO:patterns/cancer]
synonym: "malignant neoplasm of submaxillary gland" EXACT [DOID:9173]
synonym: "malignant submandibular gland neoplasm" EXACT [MONDO:patterns/cancer]
Expand All @@ -88108,13 +88112,13 @@ synonym: "malignant tumor of the submandibular gland" EXACT [DOID:9173]
synonym: "malignant tumour of submandibular gland" EXACT OMO:0003005 []
synonym: "malignant tumour of the submandibular gland" EXACT OMO:0003005 []
synonym: "submandibular gland cancer" EXACT [DOID:9173, MONDO:patterns/location, NCIT:C8396]
synonym: "submandibular gland carcinoma" EXACT [NCIT:C8396]
synonym: "submandibular gland carcinoma" NARROW [https://orcid.org/0000-0002-5002-8648, NCIT:C8396]
xref: DOID:9173 {source="MONDO:equivalentTo"}
xref: ICD10CM:C08.0 {source="DOID:9173"}
xref: ICD9:142.1 {source="DOID:9173", source="MONDO:equivalentTo", source="MONDO:i2s"}
xref: MEDGEN:57782 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C3526 {source="DOID:9173"}
xref: NCIT:C8396 {source="MONDO:equivalentTo"}
xref: NCIT:C3526 {source="https://orcid.org/0009-0001-6494-4831", source="DOID:9173", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C8396 {source="MONDO:mondoIsBroaderThanSource"}
xref: SCTID:363380002 {source="DOID:9173", source="MONDO:equivalentTo"}
xref: SCTID:94077005 {source="DOID:9173"}
xref: UMLS:C0153360 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:57782"}
Expand Down Expand Up @@ -124738,6 +124742,7 @@ xref: ICD10CM:C64-C68 {source="https://github.com/monarch-initiative/mondo/issue
xref: ICD10CM:C68.9 {source="DOID:3996"}
xref: ICD9:189.9 {source="DOID:3996"}
xref: MEDGEN:738719 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C192668 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C9297 {source="EFO:1000363", source="MONDO:equivalentTo", source="MONDO:exact-label-match"}
xref: SCTID:190132004 {source="DOID:3996"}
xref: SCTID:448233000 {source="MONDO:equivalentTo", source="DOID:3996"}
Expand Down Expand Up @@ -127666,6 +127671,7 @@ xref: MESH:D013945 {source="DOID:3284"}
xref: NANDO:2200079 {source="MONDO:NANDO", source="https://orcid.org/0000-0003-0011-764X", source="https://orcid.org/0000-0002-0170-9172"}
xref: NCIT:C7569 {source="DOID:4554", source="MONDO:equivalentTo", source="EFO:1000576"}
xref: NCIT:C7612 {source="DOID:3284"}
xref: NCIT:C7612 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: ONCOTREE:THYC {source="MONDO:equivalentTo"}
xref: Orphanet:99868 {source="MONDO:equivalentTo"}
xref: SCTID:128717008 {source="DOID:4554", source="DOID:3284"}
Expand Down Expand Up @@ -127842,7 +127848,7 @@ xref: EFO:1000585 {source="MONDO:equivalentTo", source="MONDO:EFO"}
xref: ICD9:759.2 {source="MONDO:relatedTo", source="MONDO:i2s"}
xref: MEDGEN:11810 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:D013955 {source="MONDO:equivalentTo"}
xref: NCIT:C85189 {source="MONDO:otherHierarchy", source="EFO:1000585"}
xref: NCIT:C85189 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="MONDO:otherHierarchy", source="EFO:1000585", source="https://orcid.org/0000-0002-5002-8648"}
xref: Orphanet:489 {source="MONDO:equivalentObsolete"}
xref: SCTID:39462005 {source="MONDO:equivalentTo"}
xref: UMLS:C0040124 {source="MEDGEN:11810", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
Expand Down Expand Up @@ -212440,6 +212446,7 @@ synonym: "MVA syndrome" RELATED []
synonym: "MVA1" RELATED ABBREVIATION [MONDO:Lexical]
xref: DOID:0080141 {source="MONDO:equivalentTo"}
xref: MEDGEN:338026 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C128192 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: OMIM:257300 {source="DOID:0080141", source="MONDO:equivalentTo", source="Orphanet:1052"}
xref: UMLS:C1850343 {source="MEDGEN:338026", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0000141 {source="DC-OMIM:257300", source="DOID:0080141", source="MONDO:Redundant", source="OMIM:257300"} ! mosaic variegated aneuploidy syndrome
Expand Down Expand Up @@ -405812,6 +405819,7 @@ synonym: "Pure familial AML" EXACT [Orphanet:319465]
xref: GARD:17450 {source="MONDO:GARD"}
xref: ICD10CM:C92.0 {source="Orphanet:319465/attributed", source="Orphanet:319465/ntbt", source="Orphanet:319465"}
xref: MEDGEN:1634915 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C7175 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: Orphanet:319465 {source="MONDO:equivalentTo"}
xref: SCTID:764940002 {source="MONDO:equivalentTo"}
xref: UMLS:C4707228 {source="MEDGEN:1634915", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
Expand Down Expand Up @@ -415896,7 +415904,8 @@ xref: GARD:21654 {source="MONDO:GARD"}
xref: ICD10CM:C56 {source="Orphanet:398987", source="Orphanet:398987/ntbt"}
xref: icd11.foundation:551209361 {source="MONDO:equivalentTo", source="Orphanet:398987", source="https://orcid.org/0000-0002-4142-7153"}
xref: MEDGEN:138044 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C8111 {source="MONDO:equivalentTo", source="DOID:6331"}
xref: NCIT:C39995 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C8111 {source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648", source="MONDO:preferredExternal", source="DOID:6331"}
xref: ONCOTREE:OIMT {source="MONDO:equivalentTo"}
xref: Orphanet:398987 {source="MONDO:equivalentTo"}
xref: SCTID:254871000 {source="MONDO:equivalentTo", source="DOID:6331"}
Expand Down Expand Up @@ -441726,7 +441735,8 @@ xref: ICD9:209-209.99 {source="DOID:169"}
xref: ICD9:239.7 {source="MONDO:relatedTo", source="MONDO:i2s"}
xref: MEDGEN:64652 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: MESH:D018358 {source="MONDO:equivalentTo", source="DOID:169"}
xref: NCIT:C3809 {source="MONDO:equivalentTo", source="DOID:169"}
xref: NCIT:C188218 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C3809 {source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648", source="MONDO:preferredExternal", source="DOID:169"}
xref: Orphanet:877 {source="MONDO:equivalentTo"}
xref: SCTID:128928004 {source="DOID:169"}
xref: SCTID:255046005 {source="MONDO:equivalentTo", source="DOID:169"}
Expand Down Expand Up @@ -469038,7 +469048,8 @@ synonym: "urinary tract tumor" EXACT []
synonym: "urinary tract tumour" EXACT OMO:0003005 []
xref: ICD9:239.5 {source="MONDO:relatedTo", source="MONDO:i2s"}
xref: MEDGEN:52949 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C3431 {source="MONDO:equivalentTo"}
xref: NCIT:C192666 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C3431 {source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648", source="MONDO:preferredExternal"}
xref: ONCOTREE:BLADDER {source="MONDO:equivalentTo"}
xref: SCTID:126879004 {source="MONDO:equivalentTo"}
xref: UMLS:C0042076 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:52949"}
Expand Down Expand Up @@ -547227,6 +547238,7 @@ synonym: "meningeal metastasis" EXACT [NCIT:C3814, PMID:29535794]
synonym: "metastatic malignant neoplasm in the leptomeninges" EXACT [NCIT:C3814]
xref: icd11.foundation:262966673 {source="MONDO:equivalentTo"}
xref: MEDGEN:352817 {source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
xref: NCIT:C27383 {source="https://orcid.org/0009-0001-6494-4831", source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-5002-8648"}
xref: NCIT:C3814 {source="MONDO:equivalentTo"}
xref: UMLS:C1704231 {source="MEDGEN:352817", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0024880 {source="NCIT:C3814", source="PMID:29535794"} ! metastatic malignant neoplasm
Expand Down Expand Up @@ -552180,47 +552192,6 @@ xref: UMLS:C0005944 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source=
is_a: MONDO:0005381 {source="NCIT:C97045"} ! bone disorder
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7006" xsd:anyURI

[Term]
id: MONDO:0800502
name: childhood-onset self-limited focal epilepsy syndrome
def: "A group of conditions characterized by age-dependent occurrence in otherwise normal children. Cognition and neurological evaluation are typically normal. Remission occurs in almost all patients by puberty. Presumed genetic factors have an important role. Seizure semiology and electroencephalographic (EEG) features are specific for each of the syndromes included in this group." [PMID:35503717]
synonym: "childhood-onset SeLFE" EXACT [https://www.epilepsydiagnosis.org/syndrome/epilepsy-syndrome-groupoverview.html]
is_a: MONDO:0005384 {source="https://orcid.org/0000-0002-4142-7153"} ! focal epilepsy
is_a: MONDO:0020072 {source="https://www.epilepsydiagnosis.org/syndrome/epilepsy-syndrome-groupoverview.html"} ! childhood-onset epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800498
name: childhood-onset genetic generalized epilepsy syndrome
def: "A genetic generalized epilepsy that has an onset during childhood." [https://orcid.org/0000-0001-5208-3432]
is_a: MONDO:0020072 {source="https://orcid.org/0000-0001-5208-3432"} ! childhood-onset epilepsy syndrome
is_a: MONDO:0100575 {source="https://orcid.org/0000-0002-4142-7153"} ! genetic generalized epilepsy
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800499
name: childhood-onset idiopathic generalized epilepsy syndrome
def: "An idiopathic generalized epilepsy that has an onset during childhood." [https://orcid.org/0000-0001-5208-3432]
is_a: MONDO:0005579 {source="https://orcid.org/0000-0002-4142-7153"} ! idiopathic generalized epilepsy
is_a: MONDO:0020072 {source="https://orcid.org/0000-0001-5208-3432"} ! childhood-onset epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800500
name: childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
def: "A childhood-onset epilepsy syndrome where the onset of the condition includes manifestations of cognitive, neurological, or psychiatric impairment, stagnation, or regression, due directly to the underlying etiology. In contrast, an epileptic encephalopathy (EE) is present when the encephalopathy is caused by the epileptic activity. The term developmental and epileptic encephalopathy (DEE) is used when both factors contribute to the patient’s condition." [https://www.epilepsydiagnosis.org/encephalopathy.html]
is_a: MONDO:0020072 {source="https://www.epilepsydiagnosis.org/encephalopathy.html"} ! childhood-onset epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800501
name: developmental and/or epileptic encephalopathy with spike-wave activation in sleep
def: "A spectrum of conditions with varied degree of cognitive, language, behavioral, and motor regression associated with marked spike-wave activation in sleep. The regression is seen within weeks of the EEG pattern. This syndrome encompasses the previous syndromes epileptic encephalopathy with continuous spike-wave in sleep and atypical childhood epilepsy with centrotemporal spikes (also previously known as pseudo-Lennox syndrome and atypical benign partial epilepsy). Landau–Kleffner syndrome is a specific subtype of EE-SWAS, where regression affects mainly language, with an acquired auditory agnosia." [https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html]
synonym: "DEE-SWAS" EXACT ABBREVIATION [https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html]
synonym: "EE-SWAS" EXACT ABBREVIATION [https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html]
is_a: MONDO:0800500 {source="https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html"} ! childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800487
name: variable-age onset idiopathic generalized epilepsy syndrome
Expand Down Expand Up @@ -552304,6 +552275,47 @@ synonym: "EAF" EXACT [https://www.epilepsydiagnosis.org/syndrome/adeaf-overview.
is_a: MONDO:0800492 {source="https://www.epilepsydiagnosis.org/syndrome/adeaf-overview.html"} ! variable-age onset focal epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8455" xsd:anyURI

[Term]
id: MONDO:0800498
name: childhood-onset genetic generalized epilepsy syndrome
def: "A genetic generalized epilepsy that has an onset during childhood." [https://orcid.org/0000-0001-5208-3432]
is_a: MONDO:0020072 {source="https://orcid.org/0000-0001-5208-3432"} ! childhood-onset epilepsy syndrome
is_a: MONDO:0100575 {source="https://orcid.org/0000-0002-4142-7153"} ! genetic generalized epilepsy
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800499
name: childhood-onset idiopathic generalized epilepsy syndrome
def: "An idiopathic generalized epilepsy that has an onset during childhood." [https://orcid.org/0000-0001-5208-3432]
is_a: MONDO:0005579 {source="https://orcid.org/0000-0002-4142-7153"} ! idiopathic generalized epilepsy
is_a: MONDO:0020072 {source="https://orcid.org/0000-0001-5208-3432"} ! childhood-onset epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800500
name: childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
def: "A childhood-onset epilepsy syndrome where the onset of the condition includes manifestations of cognitive, neurological, or psychiatric impairment, stagnation, or regression, due directly to the underlying etiology. In contrast, an epileptic encephalopathy (EE) is present when the encephalopathy is caused by the epileptic activity. The term developmental and epileptic encephalopathy (DEE) is used when both factors contribute to the patient’s condition." [https://www.epilepsydiagnosis.org/encephalopathy.html]
is_a: MONDO:0020072 {source="https://www.epilepsydiagnosis.org/encephalopathy.html"} ! childhood-onset epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800501
name: developmental and/or epileptic encephalopathy with spike-wave activation in sleep
def: "A spectrum of conditions with varied degree of cognitive, language, behavioral, and motor regression associated with marked spike-wave activation in sleep. The regression is seen within weeks of the EEG pattern. This syndrome encompasses the previous syndromes epileptic encephalopathy with continuous spike-wave in sleep and atypical childhood epilepsy with centrotemporal spikes (also previously known as pseudo-Lennox syndrome and atypical benign partial epilepsy). Landau–Kleffner syndrome is a specific subtype of EE-SWAS, where regression affects mainly language, with an acquired auditory agnosia." [https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html]
synonym: "DEE-SWAS" EXACT ABBREVIATION [https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html]
synonym: "EE-SWAS" EXACT ABBREVIATION [https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html]
is_a: MONDO:0800500 {source="https://www.epilepsydiagnosis.org/syndrome/ee-csws-overview.html"} ! childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0800502
name: childhood-onset self-limited focal epilepsy syndrome
def: "A group of conditions characterized by age-dependent occurrence in otherwise normal children. Cognition and neurological evaluation are typically normal. Remission occurs in almost all patients by puberty. Presumed genetic factors have an important role. Seizure semiology and electroencephalographic (EEG) features are specific for each of the syndromes included in this group." [PMID:35503717]
synonym: "childhood-onset SeLFE" EXACT [https://www.epilepsydiagnosis.org/syndrome/epilepsy-syndrome-groupoverview.html]
is_a: MONDO:0005384 {source="https://orcid.org/0000-0002-4142-7153"} ! focal epilepsy
is_a: MONDO:0020072 {source="https://www.epilepsydiagnosis.org/syndrome/epilepsy-syndrome-groupoverview.html"} ! childhood-onset epilepsy syndrome
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8490" xsd:anyURI

[Term]
id: MONDO:0810000
name: choroidal neovascularization
Expand Down

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