Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024

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	T047 T019

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SNOMEDCT/63135006	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/CSP/0725-6597	CRISP	CUI
http://purl.bioontology.org/ontology/SNMI/DA-51330	SNMI	CUI
http://purl.bioontology.org/ontology/MESH/D009468	MESH	CUI
http://purl.bioontology.org/ontology/SCTSPA/63135006	SCTSPA	CUI
http://purl.bioontology.org/ontology/MSHFRE/D009468	MSHFRE	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/63135006	SNOMEDCT	LOOM
http://purl.bioontology.org/ontology/CSP/0725-6597	CRISP	LOOM
http://purl.bioontology.org/ontology/SNMI/DA-51330	SNMI	LOOM
http://www.gamuts.net/entity#amyotonia_congenita	GAMUTS	LOOM
http://purl.obolibrary.org/obo/MONDO_0056822	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0056822	MONDO	LOOM