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DOID:0080138 - multiple congenital anomalies-hypotonia-seizures syndrome 1
Disease Ontology Definition:n_a
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0013563 - multiple congenital anomalies-hypotonia-seizures syndrome 1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)