Preferred Name

点状软骨发育不良

ID

http://purl.bmicc.cn/ontology/ICD10CN/Q77.3

cui

C0008445

free_Translation

http://purl.bioontology.org/ontology/ICD10/Q77.3

has_exact_match

http://purl.bioontology.org/ontology/ICD10/Q77.3

hasDbXref

OMIM:600121

ORDO:309789

DOID:DOID_0060292

ORDO:309796

ORDO:35173

DOID:DOID_0110851

ORDO:79344

OMIM:215100

OMIM:302950

OMIM:222765

OMIM:602497

DOID:DOID_0060293

OMIM:118650

MESH:C002806

DOID:DOID_0110853

OMIM:302960

DOID:DOID_2581

ORDO:309803

DOID:DOID_0110852

OMIM:118651

hasSTY

http://purl.bioontology.org/ontology/STY/T019

label

Q77.3 点状软骨发育不良

notation

Q77.3

prefixIRI

ICD10CN:Q77.3

prefLabel

点状软骨发育不良

tui

T019

subClassOf

http://purl.bmicc.cn/ontology/ICD10CN/Q77

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/D002806 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/OMIM/MTHU050816 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/Q77.3 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10/Q77.3 International Classification of Diseases, Version 10 CUI