U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from Gene

Items: 2

1.

Familial hyperprolactinemia

A rare genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor) in multiple affected family members. Clinically it manifests with signs usually observed in hyperprolactinemia, which are: secondary medroxyprogesterone acetate (MPA)-negative amenorrhea and galactorrhea in female patients, and hypogonadism and decreased testosterone level-driven sexual disfunction in male patients. Oligomenorrhea and primary infertility have also been reported in some female patients. [from SNOMEDCT_US]

MedGen UID:
1645317
Concept ID:
C4706551
Disease or Syndrome
2.

Multiple fibroadenoma of the breast

Fibroadenoma represents a benign breast disease characterized by lobuloalveolar growth with abnormally high proliferation of the epithelium. Patients with more than 3 fibroadenomas in 1 breast are considered to have multiple fibroadenomas (summary by Bogorad et al., 2008). [from OMIM]

MedGen UID:
816248
Concept ID:
C3809918
Neoplastic Process

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...