MCID: PRL037
MIFTS: 8

Prolactin Deficiency, Isolated

Aliases & Classifications for Prolactin Deficiency, Isolated

MalaCards integrated aliases for Prolactin Deficiency, Isolated:

Name: Prolactin Deficiency, Isolated 58 56

Characteristics:

OMIM:

58
Inheritance:
autosomal recessive


HPO:

33
prolactin deficiency, isolated:
Inheritance autosomal recessive inheritance


External Ids:

OMIM 58 264110
MedGen 43 C0271586

Summaries for Prolactin Deficiency, Isolated

MalaCards based summary : Prolactin Deficiency, Isolated An important gene associated with Prolactin Deficiency, Isolated is PRL (Prolactin). Related phenotypes are menstrual irregularities and infertility

Description from OMIM: 264110

Related Diseases for Prolactin Deficiency, Isolated

Symptoms & Phenotypes for Prolactin Deficiency, Isolated

Human phenotypes related to Prolactin Deficiency, Isolated:

33
# Description HPO Frequency HPO Source Accession
1 menstrual irregularities 33 occasional (7.5%) HP:0000858
2 infertility 33 HP:0000789
3 prolactin deficiency 33 HP:0008202

Symptoms via clinical synopsis from OMIM:

58
G U:
irregular menses
variable infertility

Lab:
no detectable prolactin secretion after stimulation with phenothiazine

Endocrine:
isolated prolactin deficiency
puerperal lactation failure

Clinical features from OMIM:

264110

Drugs & Therapeutics for Prolactin Deficiency, Isolated

Search Clinical Trials , NIH Clinical Center for Prolactin Deficiency, Isolated

Genetic Tests for Prolactin Deficiency, Isolated

Anatomical Context for Prolactin Deficiency, Isolated

Publications for Prolactin Deficiency, Isolated

Variations for Prolactin Deficiency, Isolated

Expression for Prolactin Deficiency, Isolated

Search GEO for disease gene expression data for Prolactin Deficiency, Isolated.

Pathways for Prolactin Deficiency, Isolated

GO Terms for Prolactin Deficiency, Isolated

Sources for Prolactin Deficiency, Isolated

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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