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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:204750 2-aminoadipic 2-Oxoadipic Aciduria; AMOXAD
OMIM:610006 2-methylbutyryl-Coa Dehydrogenase Deficiency
OMIM:246450 3-hydroxy-3-Methylglutaryl-Coa Lyase Deficiency; HMGCLD
OMIM:142910 3-hydroxy-3-Methylglutaryl-Coa Reductase; HMGCR
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:617248 3-methylglutaconic Aciduria, Type Viii; MGCA8
OMIM:610198 3-methylglutaconic Aciduria, Type V; MGCA5
OMIM:616271 3-methylglutaconic Aciduria with Cataracts, Neurologic Involvement, and Neutropenia; MEGCANN
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:611812 46,xx Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs;
OMIM:607080 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy
OMIM:616425 46,xy Sex Reversal 10; SRXY10
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: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)
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last database update
MGI 6.14
The Jackson Laboratory