Autosomal dominant hereditary disorder
Autosomal dominant hereditary disorder
Congenital disease
Congenital nephropathy
Congenital neurological disorder
Familial diabetes insipidus
Familial diabetes insipidus
Hereditary disorder of endocrine system
Hereditary disorder of endocrine system
Hereditary disorder of nervous system
Hereditary disorder of nervous system
Hereditary metabolic disease
Hereditary nephropathy
Hereditary nephropathy
Nephrogenic diabetes insipidus
Nephrogenic diabetes insipidus
X-linked hereditary disease
X-linked hereditary disease
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Hereditary nephrogenic diabetes insipidus (disorder)
Hereditary nephrogenic diabetes insipidus
Vasopressin-resistant diabetes insipidus
ADH-resistant diabetes insipidus
Primary nephrogenic diabetes insipidus
Familial nephrogenic diabetes insipidus
Adiuretin-resistant diabetes insipidus
Vasopressin-resistant hyposthenuria
Vasopressin-unresponsiveness hyposthenuria
Congenital nephrogenic diabetes insipidus
Renal diabetes insipidus
hereditaire nefrogene diabetes insipidus
erfelijke nefrogene diabetes insipidus
Id61165007
StatusDefined
Finding siteNeurohypophysis structure
OccurrenceCongenital
Finding siteRenal tubule structure
OccurrenceCongenital
ICD-10 complex map reference set
TargetN25.1
RuleTRUE
AdviceALWAYS N25.1
CorrelationSNOMED CT source code to target map code correlation not specified