A rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature. This includes X-linked, AR and AD forms of Aarskog syndrome. [ MONDO:cjm ]
This is just here as a test because I lose it
Term information
database
cross reference
- MedDRA:10067148 (Orphanet:915/e)
- GARD:4775 (Orphanet:915)
- Orphanet:915 (MONDO:equivalentTo)
- DOID:0111824 (MONDO:equivalentTo)
Subsets
gard_rare, rare, orphanet_rare
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/6876
https://github.com/monarch-initiative/mondo/issues/6878