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hearing loss-familial salivary gland insensitivity to aldosterone syndrome
Disease Summary
Associated Targets ()
Mondo Description Hearing loss-familial salivary gland insensitivity to aldosterone syndrome is characterised by bilateral moderate-to-severe sensorineural hearing loss and salivary gland insensitivity to aldosterone resulting in hyponatremia. It has been described in two brothers. Transmission appeared to be autosomal recessive.
Mondo Term and Equivalent IDs
MONDO:0017921: hearing loss-familial salivary gland insensitivity to aldosterone syndrome
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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.
GARD:0000422
MESH:C536927
Orphanet:3225
SCTID:716239006
MONDO:0017921
High level summary of knowledge for a disease, including descriptions and datasource references.