Title : Nephrogenic diabetes insipidus.

Pub. Date : 2017 Apr

PMID : 28134709






7 Functional Relationships(s)
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1 RECENT FINDINGS: MAGED2 mutations caused X-linked polyhydramnios with prematurity and a severe but transient form of antenatal Bartter"s syndrome.We distinguish two types of hereditary NDI: a "pure" type with loss of water only and a complex type with loss of water and ions. Water arginine vasopressin receptor 2 Homo sapiens
2 RECENT FINDINGS: MAGED2 mutations caused X-linked polyhydramnios with prematurity and a severe but transient form of antenatal Bartter"s syndrome.We distinguish two types of hereditary NDI: a "pure" type with loss of water only and a complex type with loss of water and ions. Water arginine vasopressin receptor 2 Homo sapiens
3 Mutations in the AVPR2 or AQP2 genes, encoding the vasopressin V2 receptor and the water channel Aquaporin2, respectively, lead to a "pure" NDI with loss of water but normal conservation of ions. Water arginine vasopressin receptor 2 Homo sapiens
4 Mutations in the AVPR2 or AQP2 genes, encoding the vasopressin V2 receptor and the water channel Aquaporin2, respectively, lead to a "pure" NDI with loss of water but normal conservation of ions. Water arginine vasopressin receptor 2 Homo sapiens
5 Mutations in the AVPR2 or AQP2 genes, encoding the vasopressin V2 receptor and the water channel Aquaporin2, respectively, lead to a "pure" NDI with loss of water but normal conservation of ions. Water arginine vasopressin receptor 2 Homo sapiens
6 Mutations in the AVPR2 or AQP2 genes, encoding the vasopressin V2 receptor and the water channel Aquaporin2, respectively, lead to a "pure" NDI with loss of water but normal conservation of ions. Water arginine vasopressin receptor 2 Homo sapiens
7 Mutations in the AVPR2 or AQP2 genes, encoding the vasopressin V2 receptor and the water channel Aquaporin2, respectively, lead to a "pure" NDI with loss of water but normal conservation of ions. Water arginine vasopressin receptor 2 Homo sapiens