hereditary central diabetes insipidus
subtype of central diabetes insipidus (CDI, see this term) characterized by polyuria and polydipsia due to a genetically inherited decrease in vasopressin (AVP) production
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hereditary central diabetes insipidus
Summary
hereditary central diabetes insipidus is a class of disease[1].
Key Facts
- hereditary central diabetes insipidus's instance of is recorded as class of disease[2].
- hereditary central diabetes insipidus's instance of is recorded as rare disease[3].
- hereditary central diabetes insipidus is a type of central diabetes insipidus[4].
- hereditary central diabetes insipidus is a type of endocrine system disease[5].
- hereditary central diabetes insipidus is a type of genetic disease[6].
- hereditary central diabetes insipidus is a type of pituitary deficiency[7].
- hereditary central diabetes insipidus is a type of hypopituitarism[8].
- hereditary central diabetes insipidus is part of central diabetes insipidus[9].
- hereditary central diabetes insipidus is the opposite of acquired central diabetes insipidus[10].
- hereditary central diabetes insipidus's ICPC 2 ID is recorded as T99[11].
- hereditary central diabetes insipidus's afflicts is recorded as Homo sapiens[12].
- hereditary central diabetes insipidus's afflicts is recorded as mammal[13].
- hereditary central diabetes insipidus's symptoms and signs is recorded as polyuria[14].
- hereditary central diabetes insipidus's symptoms and signs is recorded as polydipsia[15].
- hereditary central diabetes insipidus's symptoms and signs is recorded as nocturia[16].
- hereditary central diabetes insipidus's symptoms and signs is recorded as hyposthenuria[17].
- hereditary central diabetes insipidus's has cause is recorded as mutation[18].
- hereditary central diabetes insipidus's medical examination is recorded as genetic testing[19].
- hereditary central diabetes insipidus's possible treatment is recorded as medication[20].
- hereditary central diabetes insipidus's mode of inheritance is recorded as autosomal dominant[21].
- hereditary central diabetes insipidus's mode of inheritance is recorded as autosomal recessive[22].
- hereditary central diabetes insipidus's mode of inheritance is recorded as X-linked dominant[23].
- hereditary central diabetes insipidus's ICD-9-CM is recorded as 253.5[24].
- hereditary central diabetes insipidus's different from is recorded as renal glycosuria[25].
- hereditary central diabetes insipidus's health specialty is recorded as endocrinology[26].