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  2. Diabetes Insipidus

Diabetes Insipidus (Version 1.3)

Level 2: Endocrine disorders

Relevant disorders: Polydipsia, HP:0001959; Polyuria, HP:0000103
Panel types: Victorian Clinical Genetics Services, Royal Melbourne Hospital, Rare Disease
Description
This gene panel contains genetic causes of diabetes insipidus, and was developed by the RMH Endocrine Genetics clinic.
Panel Activity

2 reviewers

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

  • Bryony Thompson (Royal Melbourne Hospital)

3 Entities

3 reviewed, 3 green

List Entity Reviews Mode of inheritance Details
3 Entitiess
Green List (high evidence)
AQP2
2 reviews
2 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Diabetes insipidus, nephrogenic MIM#125800
Tags
  • clinical trial
  • treatable
Green List (high evidence)
AVP
2 reviews
2 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Diabetes insipidus, neurohypophyseal MIM#125700
Tags
  • clinical trial
  • treatable
Green List (high evidence)
AVPR2
2 reviews
2 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Diabetes insipidus, nephrogenic MIM#304800
Tags
  • clinical trial
  • SV/CNV
  • treatable

Major version comments

  • 2021-03-01 01:21 Bryony Thompson (Royal Melbourne Hospital) promoted panel to 1.0
    All genes reviewed, promote to v1.0

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

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