Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q18553373)
Watch
English
hypochromic microcytic anemia
microcytic anemia characterized by paler than normal blood cells
In more languages
edit
Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
microcytic anemia
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0050642
genetic association
STEAP3
1 reference
stated in
A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene
SLC11A2
1 reference
stated in
Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0050642
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0050642
http://identifiers.org/doid/DOID:0050642
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://purl.obolibrary.org/obo/HP_0004840
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0004840
Identifiers
MeSH descriptor ID
C536357
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0000387
C536357
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0004840
KEGG ID
H01196
0 references
Disease Ontology ID
DOID:0050642
1 reference
stated in
Disease Ontology
retrieved
29 November 2021
Disease Ontology ID
DOID:0050642
Encyclopædia Britannica Online ID
science/hypochromic-microcytic-anemia
subject named as
hypochromic microcytic anemia
0 references
Human Phenotype Ontology ID
HP:0004840
2 references
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0000387
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0004840
Mondo ID
MONDO_0000387
0 references
OMIM ID
206100
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0050642
615234
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0050642
UMLS CUI
C0271901
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0004840
UniProt disease ID
DI-01787
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
