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 ID	Human 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:620771	Jeffries-Lakhani Neurodevelopmental Syndrome; JELANS
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:620232	Joint Contractures, Osteochondromas, and B-Cell Lymphoma; JCOSL
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:618763	Joubert Syndrome 36; JBTS36
OMIM:619185	Joubert Syndrome 37; JBTS37
OMIM:619476	Joubert Syndrome 38; JBTS38
OMIM:619562	Joubert Syndrome 39; JBTS39
OMIM:608629	Joubert Syndrome 3; JBTS3
OMIM:619582	Joubert Syndrome 40; JBTS40
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:216100	Juberg-Hayward Syndrome; JHS
OMIM:244100	Jumping Frenchmen of Maine
OMIM:618795	Juvenile Arthritis; JUVAR
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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