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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
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Human Diseases/Syndromes Beginning with "J"

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

OMIM IDHuman Disease
OMIM:617988 Jaberi-Elahi Syndrome; JABELS
OMIM:123150 Jackson-Weiss Syndrome; JWS
OMIM:147791 Jacobsen Syndrome; JBS
OMIM:217080 Jalili Syndrome
OMIM:617450 Jansen-De Vries Syndrome; JDVS
OMIM:308600 Jaundice, Familial Obstructive, of Infancy
OMIM:251255 Jawad Syndrome; JWDS
OMIM:243600 Jejunal Atresia
OMIM:602551 Jejunal Atresia with Renal Adysplasia
OMIM:220400 Jervell and Lange-Nielsen Syndrome 1; JLNS1
OMIM:612347 Jervell and Lange-Nielsen Syndrome 2; JLNS2
OMIM:243800 Johanson-Blizzard Syndrome; JBS
OMIM:147770 Johnson Neuroectodermal Syndrome
OMIM:147900 Joint Laxity, Familial
OMIM:617662 Joint Laxity, Short Stature, and Myopia; JLSM
OMIM:300804 Joubert Syndrome 10; JBTS10
OMIM:614173 Joubert Syndrome 13; JBTS13
OMIM:614424 Joubert Syndrome 14; JBTS14
OMIM:614464 Joubert Syndrome 15; JBTS15
OMIM:614465 Joubert Syndrome 16; JBTS16
OMIM:614615 Joubert Syndrome 17; JBTS17
OMIM:614815 Joubert Syndrome 18; JBTS18
OMIM:213300 Joubert Syndrome 1; JBTS1
OMIM:614970 Joubert Syndrome 20; JBTS20
OMIM:615636 Joubert Syndrome 21; JBTS21
OMIM:615665 Joubert Syndrome 22; JBTS22
OMIM:616490 Joubert Syndrome 23; JBTS23
OMIM:616654 Joubert Syndrome 24; JBTS24
OMIM:616781 Joubert Syndrome 25; JBTS25
OMIM:616784 Joubert Syndrome 26; JBTS26
OMIM:617120 Joubert Syndrome 27; JBTS27
OMIM:617121 Joubert Syndrome 28; JBTS28
OMIM:608091 Joubert Syndrome 2; JBTS2
OMIM:617622 Joubert Syndrome 30; JBTS30
OMIM:617761 Joubert Syndrome 31; JBTS31
OMIM:617757 Joubert Syndrome 32; JBTS32
OMIM:617767 Joubert Syndrome 33; JBTS33
OMIM:618161 Joubert Syndrome 35; JBTS35
OMIM:608629 Joubert Syndrome 3; JBTS3
OMIM:609583 Joubert Syndrome 4; JBTS4
OMIM:610188 Joubert Syndrome 5; JBTS5
OMIM:610688 Joubert Syndrome 6; JBTS6
OMIM:611560 Joubert Syndrome 7; JBTS7
OMIM:612291 Joubert Syndrome 8; JBTS8
OMIM:612285 Joubert Syndrome 9; JBTS9
OMIM:244100 Jumping Frenchmen of Maine
OMIM:607785 Juvenile Myelomonocytic Leukemia; JMML
OMIM:175050 Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome;
OMIM:174900 Juvenile Polyposis Syndrome; JPS

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