You are using an outdated browser. Please upgrade your browser to improve your experience.
faciodigitogenital syndrome
Disease Summary
Associated Targets (2)
Tbio
2
Mondo Description 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 Term and Equivalent IDs
MONDO:0021005: faciodigitogenital syndrome
Use Cases
Submit Feedback
Download Data for faciodigitogenital syndrome
data still loading...
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MONDO:0021005
High level summary of knowledge for a disease, including descriptions and datasource references.