central diabetes insipidus

disease with impaired function of the posterior lobe of the pituitary gland, characterized by a complete or partial deficiency in the production of the hormone arginine-vasopressin (AVP) in the brain

Wikidata entity: Q12412172

P689 afflicts ... Q7377 (mammal) mammal
P689 afflicts ... Q15978631 (Homo sapiens) Homo sapiens
P2841 age of onset ... Q118907676 (any age) any age
P1889 different from ... Q124407 (type-1 diabetes) type-1 diabetes
P1889 different from ... Q126691 (gestational diabetes) gestational diabetes
P1889 different from ... Q663041 (maturity-onset diabetes of the young) maturity-onset diabetes of the young
P1889 different from ... Q929963 (primary polydipsia) primary polydipsia
P1889 different from ... Q959457 (syndrome of Inappropriate antidiuretic hormone secretion) syndrome of Inappropriate antidiuretic hormone secretion
P1889 different from ... Q1797833 (Latent autoimmune diabetes) Latent autoimmune diabetes
P1889 different from ... Q55782451 (nephrogenic syndrome of inappropriate antidiuresis) nephrogenic syndrome of inappropriate antidiuresis
P1889 different from ... Q2892779 (nephrogenic diabetes insipidus) nephrogenic diabetes insipidus
P1889 different from ... Q55790157 (dipsogenic diabetes insipidus) dipsogenic diabetes insipidus
P1889 different from ... Q55790286 (gestational diabetes insipidus) gestational diabetes insipidus
P1889 different from ... Q3025883 (type 2 diabetes) type 2 diabetes
P2176 drug or therapy used for treatment ... Q183011 (arginine vasopressin) arginine vasopressin
P2176 drug or therapy used for treatment ... Q241006 (desmopressin) desmopressin
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2888 exact match Url None ???
P2888 exact match Url None ???
P2293 genetic association ... Q14876709 (PCSK1) PCSK1
P2293 genetic association ... Q12009087 (AVP) AVP
P828 has cause ... Q133212 (tumor) tumor
P828 has cause ... Q166231 (infection) infection
P828 has cause ... Q610425 (mutation) mutation
P828 has cause ... Q192360 (autoimmunity) autoimmunity
P828 has cause ... Q594841 (idiopathy) idiopathy
P828 has cause ... Q922411 (hypopituitarism) hypopituitarism
P828 has cause ... Q56277527 (PSIS) PSIS
P828 has cause ... Q2920572 (cranial trauma) cranial trauma
P1542 has effect ... Q86 (headache) headache
P1542 has effect ... Q178436 (constipation) constipation
P1542 has effect ... Q209583 (tachycardia) tachycardia
P1542 has effect ... Q194290 (dehydration) dehydration
P1542 has effect ... Q275419 (hypotension) hypotension
P1542 has effect ... Q718113 (weight loss) weight loss
P1542 has effect ... Q1326943 (electrolyte imbalance) electrolyte imbalance
P1542 has effect ... Q6279182 (seizure) seizure
P1542 has effect ... Q1869874 (insomnia) insomnia
P1995 health specialty ... Q162606 (endocrinology) endocrinology
P1692 ICD-9-CM String 253.5 ???
P667 ICPC 2 ID String T99 ???
P31 instance of ... Q929833 (rare disease) rare disease
P923 medical examination ... Q161238 (magnetic resonance imaging) magnetic resonance imaging
P923 medical examination ... Q285223 (genetic testing) genetic testing
P923 medical examination ... Q842424 (urinalysis) urinalysis
P923 medical examination ... Q886518 (complete blood count) complete blood count
P923 medical examination ... Q886837 (blood test) blood test
P923 medical examination ... Q7201783 (plasma osmolality) plasma osmolality
P923 medical examination ... Q7900633 (urine osmolality) urine osmolality
P923 medical examination ... Q2277228 (water deprivation test) water deprivation test
P1748 NCI Thesaurus ID String C129736 ???
P1748 NCI Thesaurus ID String C84933 ???
P1448 official name Monolingualtext Arginine vasopressin deficiency ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P461 opposite of ... Q959457 (syndrome of Inappropriate antidiuretic hormone secretion) syndrome of Inappropriate antidiuretic hormone secretion
P361 part of ... Q220551 (diabetes insipidus) diabetes insipidus
P5131 possible medical findings ... Q1426443 (nocturia) nocturia
P5131 possible medical findings ... Q1641429 (hyposthenuria) hyposthenuria
P5131 possible medical findings ... Q15974799 (polyuric-polydipsic syndrome) polyuric-polydipsic syndrome
P924 possible treatment ... Q12140 (medication) medication
P1813 short name Monolingualtext AVP-D ???
P2579 studied by ... Q162606 (endocrinology) endocrinology
P279 subclass of ... Q220551 (diabetes insipidus) diabetes insipidus
P279 subclass of ... Q594841 (idiopathy) idiopathy
P279 subclass of ... Q200779 (genetic disease) genetic disease
P279 subclass of ... Q922411 (hypopituitarism) hypopituitarism
P279 subclass of ... Q4826342 (autoimmune hypophysitis) autoimmune hypophysitis
P279 subclass of ... Q18553586 (autoimmune disease of endocrine system) autoimmune disease of endocrine system
P279 subclass of ... Q2661443 (endocrine system disease) endocrine system disease
P279 subclass of ... Q56013686 (pituitary deficiency) pituitary deficiency
P780 symptoms and signs ... Q635195 (polydipsia) polydipsia
P780 symptoms and signs ... Q1124286 (polyuria) polyuria
P780 symptoms and signs ... Q1426443 (nocturia) nocturia
P780 symptoms and signs ... Q1641429 (hyposthenuria) hyposthenuria
External Ids
P2581BabelNet ID01507417n
P2581BabelNet ID01507417n
P508BNCF Thesaurus ID41937
P7647Cochrane concept IDr4hp39f2kbr5
P9272DeCS ID34283
P1036Dewey Decimal Classification616.47
P699Disease Ontology IDDOID:12388
P4746Elhuyar ZTH ID134408
P1417Encyclopædia Britannica Online IDtopic/central-diabetes-insipidus
P4317GARD rare disease ID6015
P7464Genetics Home Reference Conditions IDneurohypophyseal-diabetes-insipidus
P227GND ID4149437-4
P3841Human Phenotype Ontology IDHP:0000863
P494ICD-10 IDE23.2
P4229ICD-10-CME23.2
P7807ICD-11 ID (Foundation)1009553897
P7329ICD-11 ID (MMS)5A61.5
P493ICD-9 ID253.5
P665KEGG IDH00253
P3201Medical Dictionary for Regulatory Activities ID10068587
P3201Medical Dictionary for Regulatory Activities ID10078568
P3201Medical Dictionary for Regulatory Activities ID10012599
P3201Medical Dictionary for Regulatory Activities ID10049518
P3201Medical Dictionary for Regulatory Activities ID10068588
P3201Medical Dictionary for Regulatory Activities ID10073192
P604MedlinePlus ID000460
P604MedlinePlus ID000460
P486MeSH descriptor IDD020790
P672MeSH tree codeC12.050.351.968.419.135.750
P672MeSH tree codeC12.200.777.419.135.750
P672MeSH tree codeC12.950.419.135.750
P672MeSH tree codeC19.700.159.750
P6366Microsoft Academic ID (discontinued)2779459668
P6366Microsoft Academic ID (discontinued)2910976693
P6366Microsoft Academic ID (discontinued)2911134924
P5270Mondo IDMONDO_0015790
P691NL CR AUT IDph640585
P492OMIM ID125700
P492OMIM ID125700
P492OMIM ID304900
P492OMIM ID304900
P1550Orphanet ID178029
P4233PatientsLikeMe condition IDdiabetes-insipdus
P10376ScienceDirect topic IDmedicine-and-dentistry/diabetes-insipidus
P5806SNOMED CT ID45369008
P5082Store medisinske leksikon IDdiabetes_insipidus
P2892UMLS CUIC0687720
P11143WikiProjectMed IDCentral_diabetes_insipidus
P3471WikiSkripta article ID20245

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