PROLACTIN DEFICIENCY, ISOLATED

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr:
OMIM Id: 264110
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal recessive inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0000858) Menstrual irregularities Occasional [HPO:probinson] 42 / 7739
2
(HPO:0000789) Infertility 74 / 7739
3
(HPO:0008202) Prolactin deficiency 3 / 7739
4
(OMIM) Variable infertility 1 / 7739
5
(OMIM) Isolated prolactin deficiency 1 / 7739
6
(OMIM) No detectable prolactin secretion after stimulation with phenothiazine 1 / 7739
7
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
8
(OMIM) Puerperal lactation failure 1 / 7739
9
(OMIM) Irregular menses 2 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: