Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

SCLERODERMA, FAMILIAL PROGRESSIVE
Synonyms

CREST SYNDROME
ID

http://purl.bioontology.org/ontology/OMIM/181750
altLabel

CREST SYNDROME

SYSTEMIC SCLEROSIS, SUSCEPTIBILITY TO
cui

C1866983

C0206138
MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.
notation

181750
OMIM Entry Type

5
OMIM MimType Value

perc
prefLabel

SCLERODERMA, FAMILIAL PROGRESSIVE
tui

T047
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http://purl.bmicc.cn/ontology/ICD10CN/M34.1 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10CM/M34.1 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D017675 Medical Subject Headings CUI