Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Jump to:
Spinner 000000 16px loading...
Preferred Name

VALINEMIA
Synonyms

VALINE TRANSAMINASE DEFICIENCY
ID

http://purl.bioontology.org/ontology/OMIM/277100
altLabel

VALINE TRANSAMINASE DEFICIENCY

HYPERVALINEMIA
cui

C0268573
MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.
notation

277100
OMIM Entry Type

5
OMIM MimType Value

perc
prefLabel

VALINEMIA
tui

T047
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/E71.19 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/C536524 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C536524 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/LNC/LA12503-1 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/LNC/LA12503-1 Logical Observation Identifier Names and Codes LOOM