|
DOID:0080139 - multiple congenital anomalies-hypotonia-seizures syndrome 2
Disease Ontology Definition:n_a
Synonyms:
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:300868 - multiple congenital anomalies-hypotonia-seizures syndrome 2; mcahs2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)