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Disease Ontology Browser
Meckel syndrome (DOID:0050778)
Alliance: disease page
Synonyms: Meckel-Gruber syndrome
Alt IDs: OMIM:249000, OMIM:267010, OMIM:603194, OMIM:607361, OMIM:611134, OMIM:611561, OMIM:612284, OMIM:613885, OMIM:614175, OMIM:614209, OMIM:615397, ICD9CM:753.1, ICD9CM:753.10, ORDO:564, UMLS_CUI:C0311245
Definition: A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia.

Disease References using Mouse Models (12)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory