BioAssay Ontology / 生物活性分析本体

Last uploaded: September 7, 2023
Preferred Name

Camurati-Engelmann disease

Synonyms

Diaphyseal dysplasia

Definitions

Xref MGI. OMIM mapping confirmed by DO. [SN]. An osteosclerosis that has_material_basis_in mutations in the TGFB1 gene which results_in increased bone density located_in long bone.

ID

http://purl.obolibrary.org/obo/DOID_4997

comment

Xref MGI. OMIM mapping confirmed by DO. [SN].

database_cross_reference

OMIM:606631

ICD10CM:Q78.3

SNOMEDCT_US_2020_03_01:34643004

OMIM:131300

NCI:C84610

GARD:1072

MESH:D003966

UMLS_CUI:C0011989

has exact synonym

Diaphyseal dysplasia

Engelman's disease

progressive diaphyseal dysplasia

id

DOID:4997

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus

label

Camurati-Engelmann disease

notation

DOID:4997

prefLabel

Camurati-Engelmann disease

textual definition

An osteosclerosis that has_material_basis_in mutations in the TGFB1 gene which results_in increased bone density located_in long bone.

引自

http://purl.obolibrary.org/obo/doid.owl

有_obo_命名空间

disease_ontology

subClassOf

http://purl.obolibrary.org/obo/DOID_4254

http://purl.obolibrary.org/obo/DOID_0050177

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http://purl.bioontology.org/ontology/OMIM/131300 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/DOID_4997 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/DOID_4997 Human Disease Ontology / 人类疾病本体 SAME_URI
http://www.orpha.net/ORDO/Orphanet_1328 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0007542 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0007542 Experimental Factor Ontology / 实验性因素本体 LOOM