Preferred Name |
ACHARD SYNDROME |
ID |
http://purl.bioontology.org/ontology/OMIM/100700 |
cui |
C1332135 |
MIMTYPEMEANING |
Other, mainly phenotypes with suspected mendelian basis |
notation |
100700 |
OMIM Entry Type |
0 |
OMIM MimType Value |
none |
prefLabel |
ACHARD SYNDROME |
tui |
T047 |