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Items: 12

1.

Polyploidy

A numerical chromosomal abnormality characterized by the presence of more than two sets of chromosomes. [from NCI]

MedGen UID:
18567
Concept ID:
C0032578
Cell or Molecular Dysfunction
2.

Catastrophic antiphospholipid syndrome

MedGen UID:
910984
Concept ID:
CN242096
Disease or Syndrome
3.

Indicated

MedGen UID:
731837
Concept ID:
C1444656
Finding
4.

Independent

MedGen UID:
721426
Concept ID:
C1299583
Finding
5.

Cryopyrin associated periodic syndrome

A group of autoinflammatory syndromes caused by mutations in the NLRP3 gene. Signs and symptoms include rash, fever, headache, joint pain, conjunctivitis, and weakness. The symptoms may exacerbate with exposure to cold weather. [from NCI]

MedGen UID:
412215
Concept ID:
C2316212
Disease or Syndrome
6.

Maternal

A designation that has some relationship to motherhood. [from NCI]

MedGen UID:
348949
Concept ID:
C1858460
Finding
7.

Acute fatty liver of pregnancy

Acute fatty liver of pregnancy is a rare but severe complication occurring in the third trimester of pregnancy or in early postpartum period bearing a risk for perinatal and maternal mortality with manifestations of jaundice, rise of hepatic injuries and evolving to acute liver failure and encephalopathy. [from SNOMEDCT_US]

MedGen UID:
264102
Concept ID:
C1455728
Disease or Syndrome
8.

Examined for

Having been subjected to inspection or evaluation. [from NCI]

MedGen UID:
83047
Concept ID:
C0332128
Finding
9.

Phosphate

Inorganic salts of phosphoric acid. [from MeSH]

MedGen UID:
18434
Concept ID:
C0031603
Inorganic Chemical; Pharmacologic Substance
10.

Heredity

The transmission of traits encoded in GENES from parent to offspring. [from MeSH]

MedGen UID:
6814
Concept ID:
C0019266
Molecular Function
11.

Chromosomal anomaly

Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. [from MeSH]

MedGen UID:
954
Concept ID:
C0008625
Cell or Molecular Dysfunction
12.

One or more systems examined

MedGen UID:
600392
Concept ID:
C0420618
Finding
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