Autosomal dominant primary hypomagnesemia with hypocalciuria

Source codes that map to this concept

1 source code normalizes to Autosomal dominant primary hypomagnesemia with hypocalciuria via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Autosomal dominant primary hypomagnesemia with hypocalciuria across source vocabularies.

• Autosomal dominant primary hypomagnesaemia with hypocalciuria
• Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)
• hipomagnesemia primaria autosómica dominante con hipocalciuria
• hipomagnesemia primaria autosómica dominante con hipocalciuria (trastorno)
• HOMG2 - renal hypomagnesaemia type 2
• HOMG2 - renal hypomagnesemia type 2
• Isolated autosomal dominant hypomagnesaemia
• Isolated autosomal dominant hypomagnesemia
• Isolated renal magnesium wasting

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Get this concept via the API

Resolve Autosomal dominant primary hypomagnesemia with hypocalciuria - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.

curl "https://api.omophub.com/v1/concepts/37110873?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"