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Human Disease and Mouse Model Detail
Human Disease Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies; MURCS
OMIM ID: 601076
Human Phenotype Ontology associations
Synonyms Klippel-Feil Deformity, Conductive Deafness, and Absent Vagina; Mayer-Rokitansky-Kuster-Hauser Syndrome, Type II; Mrkh, Type II
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory