About   Help   FAQ
Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character
 
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
 

Human Diseases/Syndromes Beginning with "0-9"

To see all annotations for a disease, click the disease name.

OMIM IDHuman Disease
OMIM:264300 17-beta Hydroxysteroid Dehydrogenase III Deficiency
OMIM:616034 2,4-dienoyl-Coa Reductase Deficiency; DECRD
OMIM:610006 2-methylbutyryl-Coa Dehydrogenase Deficiency
OMIM:246450 3-hydroxy-3-Methylglutaryl-Coa Lyase Deficiency; HMGCLD
OMIM:605911 3-hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency; HMGCS2D
OMIM:231530 3-hydroxyacyl-Coa Dehydrogenase Deficiency
OMIM:236795 3-hydroxyisobutyric Aciduria
OMIM:250620 3-hydroxyisobutyryl-Coa Hydrolase Deficiency; HIBCHD
OMIM:257920 3mc Syndrome 1; 3MC1
OMIM:265050 3mc Syndrome 2; 3MC2
OMIM:248340 3mc Syndrome 3; 3MC3
OMIM:210200 3-methylcrotonyl-Coa Carboxylase 1 Deficiency; MCC1D
OMIM:210210 3-methylcrotonyl-Coa Carboxylase 2 Deficiency; MCC2D
OMIM:258501 3-methylglutaconic Aciduria, Type III; MGCA3
OMIM:250950 3-methylglutaconic Aciduria, Type I; MGCA1
OMIM:250951 3-methylglutaconic Aciduria, Type IV; MGCA4
OMIM:617698 3-methylglutaconic Aciduria, Type IX; MGCA9
OMIM:619835 3-methylglutaconic Aciduria, Type Viia; MGCA7A
OMIM:616271 3-methylglutaconic Aciduria, Type Viib; MGCA7B
OMIM:617248 3-methylglutaconic Aciduria, Type Viii; MGCA8
OMIM:610198 3-methylglutaconic Aciduria, Type V; MGCA5
OMIM:614739 3-methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome; MEGDEL
OMIM:400045 46,xx Sex Reversal 1; SRXX1
OMIM:278850 46,xx Sex Reversal 2; SRXX2
OMIM:300833 46,xx Sex Reversal 3; SRXX3
OMIM:617480 46,xx Sex Reversal 4; SRXX4
OMIM:618901 46,xx Sex Reversal 5; SRXX5
OMIM:611812 46,xx Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs;
OMIM:607080 46,xy Gonadal Dysgenesis with Minifascicular Neuropathy; GDMN
OMIM:616425 46,xy Sex Reversal 10; SRXY10
OMIM:273250 46,xy Sex Reversal 11; SRXY11
OMIM:400044 46,xy Sex Reversal 1; SRXY1
OMIM:300018 46,xy Sex Reversal 2; SRXY2
OMIM:612965 46,xy Sex Reversal 3; SRXY3
OMIM:154230 46,xy Sex Reversal 4; SRXY4
OMIM:613080 46,xy Sex Reversal 5; SRXY5
OMIM:613762 46,xy Sex Reversal 6; SRXY6
OMIM:233420 46,xy Sex Reversal 7; SRXY7
OMIM:614279 46,xy Sex Reversal 8; SRXY8
OMIM:616067 46,xy Sex Reversal 9; SRXY9
OMIM:143460 5-hydroxytryptamine Oxygenase Regulator; HTOR
OMIM:260005 5-oxoprolinase Deficiency; OPLAHD
OMIM:619199 6-phosphogluconate Dehydrogenase Deficiency; PGDD
OMIM:172150 6-phosphogluconolactonase Deficiency

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory