Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

AMYOTONIA CONGENITA

Synonyms

OPPENHEIM DISEASE

ID

http://purl.bioontology.org/ontology/OMIM/205000

altLabel

OPPENHEIM DISEASE

cui

C0002735

MIMTYPEMEANING

Other, mainly phenotypes with suspected mendelian basis

notation

205000

OMIM Entry Type

0

OMIM MimType Value

none

prefLabel

AMYOTONIA CONGENITA

tui

T019

T047

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http://purl.bioontology.org/ontology/MESH/D009468 Medical Subject Headings CUI