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Online Mendelian Inheritance in Man
Last uploaded:
August 28, 2024
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Preferred Name | HYPERPROLACTINEMIA | |
Synonyms |
HPRL |
|
ID |
http://purl.bioontology.org/ontology/OMIM/615555 |
|
altLabel |
HPRL
|
|
cui |
C0020514
|
|
Gene Locus |
5p13.2
|
|
Gene Symbol |
HPRL MFAB PRLR
|
|
Has manifestation |
http://purl.bioontology.org/ontology/OMIM/MTHU006969 http://purl.bioontology.org/ontology/OMIM/MTHU009110 http://purl.bioontology.org/ontology/OMIM/MTHU004754 http://purl.bioontology.org/ontology/OMIM/MTHU044629 |
|
MIMTYPEMEANING |
Phenotype description, molecular basis known.
|
|
notation |
615555
|
|
OMIM Entry Type |
3
|
|
OMIM MimType Value |
pound
|
|
prefLabel |
HYPERPROLACTINEMIA
|
|
Scope Statement |
Caused by mutation in the prolactin receptor gene (PRLR, 176761.0002) [MOLECULAR BASIS]
|
|
tui |
T047
|
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