Kidney Tissue Atlas Ontology

Last uploaded: March 16, 2024
Preferred Name

neurohypophyseal diabetes insipidus
Synonyms

diabetes insipidus, cranial type

diabetes insipidus, primary central

hereditary central diabetes insipidus

diabetes insipidus, neurohypophyseal

diabetes insipidus of pituitary gland

neurogenic diabetes insipidus

Arginine vasopressin deficiency

pituitary gland diabetes insipidus

central diabetes insipidus

AVP deficiency

hereditary CDI

hereditary neurogenic diabetes insipidus

pituitary diabetes insipidus

antidiuretic hormone deficiency

vasopressin deficiency

ADH deficiency

vasopressin defective diabetes insipidus

Definitions

Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis.

ID

http://purl.obolibrary.org/obo/MONDO_0007450

closeMatch

http://identifiers.org/snomedct/190484000

http://identifiers.org/snomedct/154699008

http://identifiers.org/snomedct/64410003

http://identifiers.org/snomedct/267393007

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/location.yaml

database_cross_reference

NCIT:C84933

OMIM:125700

Orphanet:30925

ICD10:E23.2

SCTID:45369008

DOID:12388

disease has basis in dysfunction of

http://identifiers.org/hgnc/894

exactMatch

http://identifiers.org/omim/125700

http://purl.obolibrary.org/obo/DOID_12388

http://identifiers.org/snomedct/45369008

http://purl.obolibrary.org/obo/NCIT_C84933

http://www.orpha.net/ORDO/Orphanet_30925

has exact synonym

diabetes insipidus of pituitary gland

neurogenic diabetes insipidus

Arginine vasopressin deficiency

pituitary gland diabetes insipidus

central diabetes insipidus

AVP deficiency

hereditary CDI

hereditary neurogenic diabetes insipidus

pituitary diabetes insipidus

antidiuretic hormone deficiency

vasopressin deficiency

ADH deficiency

vasopressin defective diabetes insipidus

has related synonym

diabetes insipidus, cranial type

diabetes insipidus, primary central

hereditary central diabetes insipidus

diabetes insipidus, neurohypophyseal

id

MONDO:0007450

imported from

http://purl.obolibrary.org/obo/mondo.owl

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_clinical_subtype

label

neurohypophyseal diabetes insipidus

notation

MONDO:0007450

prefLabel

neurohypophyseal diabetes insipidus

textual definition

Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0015790

http://purl.obolibrary.org/obo/MONDO_0004782

http://purl.obolibrary.org/obo/MONDO_0000426

http://purl.obolibrary.org/obo/MONDO_0019117

http://purl.obolibrary.org/obo/MONDO_0003381

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