hereditary stomatocytosis (Q3973817): Difference between revisions

From Wikidata

Jump to navigation Jump to search

Browse history interactively

← Older editNewer edit →

Revision as of 22:52, 16 December 2018 (restore) Andreasmperu (talk | contribs) Administrators 451,626 edits ‎Added [es] label: estomatocitosis hereditaria ← Older edit		Revision as of 19:23, 25 February 2024 (restore) undo KrBot (talk | contribs) Bots, IP block exemptions, Rollbackers 70,939,605 edits ‎Changed reference of claim: UMLS CUI (P2892): C1262483, см. / see autofix на / on Property talk:P5270 Newer edit →
(24 intermediate revisions by 14 users not shown)
label / ar		label / ar
	Hereditary stomatocytosis		كثرة الكريات المفوهة الوراثية
label / ja		label / ja
			遺伝性有口赤血球症
aliases / ar / 0		aliases / ar / 0
			Hereditary stomatocytosis
description / uk		description / uk
			хвороба людини
description / hy		description / hy
			մարդու հիվանդություն
		Property / Orphanet ID: 98365 / reference
			stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO_0020102
Property / Orphanet ID: 98365 / reference
	stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO:0020102
		Property / subclass of: hereditary haemolytic anaemia due to red cell membrane defects / reference
			stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO_0020102
Property / subclass of: hereditary haemolytic anaemia due to red cell membrane defects / reference
	stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO:0020102
		Property / ICD-10-CM: D58.8 / reference
			stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO_0020102
Property / ICD-10-CM: D58.8 / reference
	stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO:0020102
		Property / ICD-9-CM: 282.8 / reference
			stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO_0020102
Property / ICD-9-CM: 282.8 / reference
	stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO:0020102
Property / Mondo ID
	MONDO:0020102
Property / Mondo ID: MONDO:0020102 / rank
	Normal rank
Property / Mondo ID: MONDO:0020102 / reference
	stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO:0020102
		Property / UMLS CUI: C1262483 / reference
			stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO_0020102
Property / UMLS CUI: C1262483 / reference
	stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018 Timestamp +2018-07-28T00:00:00Z Timezone +00:00 Calendar Gregorian Precision 1 day Before 0 After 0 Mondo ID: MONDO:0020102
		Property / Commons category
			Hereditary stomatocytosis
		Property / Commons category: Hereditary stomatocytosis / rank
			Normal rank
		Property / instance of
			rare disease
		Property / instance of: rare disease / rank
			Normal rank
		Property / instance of
			class of disease
		Property / instance of: class of disease / rank
			Normal rank
		Property / genetic association
			RHAG
		Property / genetic association: RHAG / rank
			Normal rank
		Property / genetic association: RHAG / reference
			stated in: The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein
		Property / Microsoft Academic ID
			2779412095
		Property / Microsoft Academic ID: 2779412095 / rank
			Normal rank
		Property / KEGG ID
			H00232
		Property / KEGG ID: H00232 / rank
			Normal rank
		Property / ICD-11 (foundation)
			2067120097
		Property / ICD-11 (foundation): 2067120097 / rank
			Normal rank
		Property / WikiProjectMed ID
			Hereditary stomatocytosis
		Property / WikiProjectMed ID: Hereditary stomatocytosis / rank
			Normal rank
		Property / Mondo ID
			MONDO_0020102
		Property / Mondo ID: MONDO_0020102 / rank
			Normal rank
links / commonswiki / name		links / commonswiki / name
			Category:Hereditary stomatocytosis
links / arwiki / name		links / arwiki / name
			كثرة الكريات المفوهة الوراثية

---

Revision as of 19:23, 25 February 2024

human disease

• Hereditary stomatocytic disease

Language	Label	Description	Also known as
English	hereditary stomatocytosis	human disease	Hereditary stomatocytic disease

Statements

instance of

rare disease

0 references

class of disease

0 references

subclass of

poikilocytosis

0 references

hereditary haemolytic anaemia due to red cell membrane defects

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0020102

health specialty

hematology

0 references

symptoms and signs

stomatocyte

0 references

genetic association

RHAG

1 reference

stated in

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein

ICD-9-CM

282.8

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0020102

exact match

http://www.orpha.net/ORDO/Orphanet_98365

0 references

Commons category

Hereditary stomatocytosis

0 references

Identifiers

KEGG ID

H00232

0 references

DiseasesDB

29710

1 reference

imported from Wikimedia project

English Wikipedia

ICD-10

D58.8

1 reference

imported from Wikimedia project

English Wikipedia

ICD-10-CM

D58.8

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0020102

ICD-11 (foundation)

2067120097

0 references

ICD-9 ID

282.8

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

2779412095

0 references

Mondo ID

MONDO_0020102

0 references

OMIM ID

185000

1 reference

imported from Wikimedia project

English Wikipedia

185010

1 reference

imported from Wikimedia project

English Wikipedia

Orphanet ID

98365

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0020102

UMLS CUI

C1262483

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0020102

WikiProjectMed ID

Hereditary stomatocytosis

0 references

 

Sitelinks

Wikipedia(3 entries)

• arwiki كثرة الكريات المفوهة الوراثية
• enwiki Hereditary stomatocytosis
• itwiki Stomatocitosi ereditaria

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

• commonswiki Category:Hereditary stomatocytosis

Retrieved from "https://www.wikidata.org/w/index.php?title=Q3973817&oldid=2087119183"