CM2
ARNOLD-CHIARI MALFORMATION
http://purl.bioontology.org/ontology/OMIM/207950
C0003803
C0555206
http://purl.bioontology.org/ontology/OMIM/MTHU002588
http://purl.bioontology.org/ontology/OMIM/MTHU000300
http://purl.bioontology.org/ontology/OMIM/MTHU027680
http://purl.bioontology.org/ontology/OMIM/MTHU023662
http://purl.bioontology.org/ontology/OMIM/MTHU023668
http://purl.bioontology.org/ontology/OMIM/MTHU011163
http://purl.bioontology.org/ontology/OMIM/MTHU000197
http://purl.bioontology.org/ontology/OMIM/MTHU023664
http://purl.bioontology.org/ontology/OMIM/MTHU002499
http://purl.bioontology.org/ontology/OMIM/MTHU023666
http://purl.bioontology.org/ontology/OMIM/MTHU022605
http://purl.bioontology.org/ontology/OMIM/MTHU012819
http://purl.bioontology.org/ontology/OMIM/MTHU041713
http://purl.bioontology.org/ontology/OMIM/MTHU036443
http://purl.bioontology.org/ontology/OMIM/MTHU011847
http://purl.bioontology.org/ontology/OMIM/MTHU023663
http://purl.bioontology.org/ontology/OMIM/MTHU022741
http://purl.bioontology.org/ontology/OMIM/MTHU004807
http://purl.bioontology.org/ontology/OMIM/MTHU067481
http://purl.bioontology.org/ontology/OMIM/MTHU067480
http://purl.bioontology.org/ontology/OMIM/MTHU001330
http://purl.bioontology.org/ontology/OMIM/MTHU036349
http://purl.bioontology.org/ontology/OMIM/MTHU027679
http://purl.bioontology.org/ontology/OMIM/MTHU023665
http://purl.bioontology.org/ontology/OMIM/MTHU000235
Mendelian phenotype or locus, molecular basis unknown.
207950
5
perc
CHIARI MALFORMATION TYPE II
Symptom onset at birth or infancy Arnold-Chiari type II is uniquely associated with myelomeningocele (182940) [MISCELLANEOUS]
T019