Preferred Name |
Parotid Aplasia or Hypoplasia |
ID |
http://purl.bioontology.org/ontology/MESH/C566702 |
cui |
C1867059 |
HM |
D010305 D010306 |
Inverse of RB |
0 |
Mapped to | |
MDA |
20121105 |
MeSH Frequency |
1 |
notation |
C566702 |
prefLabel |
Parotid Aplasia or Hypoplasia |
SC |
3 |
TERMUI |
T832718 |
TH |
OMIM (2013) |
tui |
T047 |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/OMIM/180920 | Online Mendelian Inheritance in Man | CUI |