About: leiomyomatosis

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human disease

Attributes	Values
rdf:type	Item
description	Krankheit (de) Human disease (en) хвороба людини (uk) مرض يصيب الإنسان (ar)
exact match	wds:Q18556640-F3076B35-20FD-4462-AA07-4B31EA18639F wds:Q18556640-FFFDB224-8284-4F40-A250-3818780F693B
exact match	http://purl.obolibrary.org/obo/DOID_5138 http://identifiers.org/doid/DOID:5138
health specialty	wds:Q18556640-65CBEBF8-6230-4268-A2F9-73DC2AD38BED
Mondo ID	wds:Q18556640-7739A5B5-50C7-419C-A1F9-1DA25C5AAAB3
Disease Ontology ID	wds:Q18556640-D1AB456F-F21E-4A62-902A-110D5A55432E
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0003295
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:5138
health specialty	oncology
Mondo ID	MONDO_0003295
Disease Ontology ID	DOID:5138
rdfs:label	leiomyomatosis (en) léiomyomatose (fr)
skos:prefLabel	leiomyomatosis (en) léiomyomatose (fr)
name	leiomyomatosis (en) léiomyomatose (fr)
instance of	wds:Q18556640-883B9AED-5551-4F4A-97A6-CFE1AC5B757B
instance of	class of disease
subclass of	wds:Q18556640-D4CFC5B5-EBB1-4AF8-82A9-3D804A00E819
subclass of	leiomyoma
skos:altLabel	leiomyomatosis, no ICD-O subtype (morphologic abnormality) (en) Leiomyomatosis (en) leiomyomatosis, no ICD-O subtype (en)
NCI Thesaurus ID	wds:Q18556640-826E0612-BD4E-4C2B-9FEE-157F5A6FCF25
UMLS CUI	wds:Q18556640-5B62167C-635C-46EA-8F74-606736F9774B wds:Q18556640-B017583D-7377-420F-B705-5143348A34F1
MeSH descriptor ID	wds:Q18556640-54257EAC-BB56-4DB3-9F07-97EBA9BBD67A
on focus list of Wikimedia project	wds:Q18556640-42F3C8F3-001E-49DE-A463-45FC3CCD6204
MeSH tree code	wds:Q18556640-CFAA4B28-B0DE-4E67-99F1-DE8FE42AE9BD
ICD-11 ID (MMS)	wds:Q18556640-a852d430-159b-44bc-8d03-4c295b7b6db9
ICD-11 (foundation)	wds:Q18556640-BDF928B2-A3B7-469A-90E3-F9088075156C
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D018231
MeSH tree code	http://id.nlm.nih.gov/mesh/C04.557.450.590.450.465
NCI Thesaurus ID	C3748
UMLS CUI	C0206654 C0728890
MeSH descriptor ID	D018231
on focus list of Wikimedia project	WikiProject Medicine
MeSH tree code	C04.557.450.590.450.465
ICD-11 ID (MMS)	XH60C2
ICD-11 (foundation)	617489082
ICD-O	wds:Q18556640-E645E517-58E5-434C-9668-3AB8BB209D43
ICD-O	8890/1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18556640
is subclass of of	intravenous leiomyomatosis familial leiomyomatosis diffuse leiomyomatosis syndrome uterine corpus leiomyomatosis diffuse peritoneal leiomyomatosis
is subclass of of	wds:Q19000779-a9148113-4acc-2015-a31c-03ab2869984f wds:Q55790432-E4B86FDF-109C-4742-9ECC-A5AFD780616A wds:Q18556975-8F2E22B9-2325-47A7-97FA-F89942F4135A wds:Q16966324-0055E0EA-48E6-4D30-84DF-FE32DCB2EBA0 wds:Q18557067-B9844646-C9A4-47A2-BA56-A30A39913B2F
is main subject of	Leiomyomatosis peritonealis disseminata coexisting with endometriosis within the same lesions: a case report with review of the literature Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma Parasitic peritoneal leiomyomatosis diagnosed 6 years after laparoscopic myomectomy with electric tissue morcellation: report of a case and review of the literature. Disseminated peritoneal leiomyomatosis with endometriosis. MR and CT findings of leiomyomatosis peritonealis disseminata with emphasis on assisted reproductive technology as a risk factor. Disseminated peritoneal leiomyomatosis: an unusual complication of laparoscopic myomectomy. LDH-A inhibition, a therapeutic strategy for treatment of hereditary leiomyomatosis and renal cell cancer Increasing reactive oxygen species as a therapeutic approach to treat hereditary leiomyomatosis and renal cell carcinoma Adrenal nodular hyperplasia in hereditary leiomyomatosis and renal cell cancer Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families Type IV collagen: structure, gene organization, and role in human diseases. Molecular basis of Goodpasture and Alport syndromes and diffuse leiomyomatosis Retroperitoneal leiomyomatosis: a case report Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndrome Intracardiac leiomyomatosis: a comprehensive analysis of 194 cases Evidence for a new fumarate hydratase gene mutation in a unilateral type 2 segmental leiomyomatosis Intracardiac leiomyomatosis: echocardiographic features Leiomyoblastoma and leiomyomatosis of the small intestine in a case of von Recklinghausen's disease Pelvic leiomyomatosis with intracaval and intracardiac extension: a case report and review of the literature Intravenous uterine leiomyomatosis with right heart extension: successful two-stage surgical removal Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America Hereditary leiomyomatosis and renal cell carcinoma Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer Morphologic and molecular characteristics of uterine leiomyomas in hereditary leiomyomatosis and renal cancer (HLRCC) syndrome Multiple cutaneous and uterine leiomyomatosis syndrome: a review Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer. Hereditary leiomyomatosis and renal cell cancer: a syndrome associated with an aggressive form of inherited renal cancer Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient The morphologic spectrum of kidney tumors in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC) Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's Syndrome) Diffuse esophageal leiomyomatosis in a patient with Alport syndrome: CT demonstration LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis Combination of pulmonary lymphangioleiomyomatosis with skin leiomyomatosis and uterine leiomyoma Pathophysiology and possible iatrogenic cause of leiomyomatosis peritonealis disseminata

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