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Items: 4

1.

Aortic valve calcification

Deposition of calcium salts in the aortic valve. [from HPO]

MedGen UID:
140899
Concept ID:
C0428791
Disease or Syndrome; Finding
2.

Congenital bilateral aplasia of vas deferens from CFTR mutation

Cystic fibrosis (CF) is a multisystem disease affecting epithelia of the respiratory tract, exocrine pancreas, intestine, hepatobiliary system, and exocrine sweat glands. Morbidities include recurrent sinusitis and bronchitis, progressive obstructive pulmonary disease with bronchiectasis, exocrine pancreatic deficiency and malnutrition, pancreatitis, gastrointestinal manifestations (meconium ileus, rectal prolapse, distal intestinal obstructive syndrome), liver disease, diabetes, male infertility due to hypoplasia or aplasia of the vas deferens, and reduced fertility or infertility in some women. Pulmonary disease is the major cause of morbidity and mortality in CF. [from GeneReviews]

MedGen UID:
98021
Concept ID:
C0403814
Congenital Abnormality
3.

Platelet-type bleeding disorder 12

Platelet prostaglandin-endoperoxidase synthase-1 deficiency is a hematologic disorder characterized by mildly increased bleeding due to a platelet defect. The PTGS1 gene (176805) encodes prostaglandin-endoperoxidase synthase-1, also known as COX1 or PGHS1, which catalyzes the formation of prostaglandin G2 (PGG2) and prostaglandin H2 from arachidonic acid, and the downstream formation of thromboxane A2 (TXA2) and prostacyclin. Thromboxane A2 is important for platelet aggregation (summary by Matijevic-Aleksic et al., 1996). [from OMIM]

MedGen UID:
414043
Concept ID:
C2751535
Disease or Syndrome
4.

Cardiac valve calcification

Abnormal calcification of a cardiac valve. [from HPO]

MedGen UID:
383924
Concept ID:
C1856483
Finding
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