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Items: 12

1.

Absence

MedGen UID:
739164
Concept ID:
C1689985
Anatomical Abnormality
2.

Retraction

MedGen UID:
568395
Concept ID:
C0332523
Finding
3.

Neuronal loss in central nervous system

MedGen UID:
342515
Concept ID:
C1850496
Finding
4.

Degenerative abnormality

Disturbance of cell integrity and deterioration of normal tissue, cells or organs. [from NCI_CDISC]

MedGen UID:
3705
Concept ID:
C0011164
Pathologic Function
5.

beta-Galactosidase

A group of enzymes that catalyzes the hydrolysis of terminal, non-reducing beta-D-galactose residues in beta-galactosides. Deficiency of beta-Galactosidase A1 may cause GANGLIOSIDOSIS, GM1. [from MeSH]

MedGen UID:
550
Concept ID:
C0005220
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
6.

Endoglycosidases

MedGen UID:
760845
Concept ID:
C3537242
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
7.

Lactogest

MedGen UID:
327777
Concept ID:
C1564492
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
8.

Dairyaid

MedGen UID:
289840
Concept ID:
C1564491
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
9.

Lactrase

MedGen UID:
152475
Concept ID:
C0721296
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
10.

Lactaid

MedGen UID:
149213
Concept ID:
C0733877
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
11.

Neurodegenerative disease

Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures. [from MeSH]

MedGen UID:
101195
Concept ID:
C0524851
Disease or Syndrome
12.

Glycosidase

covering the sugar hydrolases. [from CRISP]

MedGen UID:
5349
Concept ID:
C0017976
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
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