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Items: 1 to 20 of 22

1.

Leukemia

A cancer of the blood and bone marrow characterized by an abnormal proliferation of leukocytes. [from HPO]

MedGen UID:
9725
Concept ID:
C0023418
Neoplastic Process
2.

peptide A

MedGen UID:
139453
Concept ID:
C0388060
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
3.

Ion exchange

Reversible chemical reaction between a solid, often one of the ION EXCHANGE RESINS, and a fluid whereby ions may be exchanged from one substance to another. This technique is used in water purification, in research, and in industry. [from MeSH]

MedGen UID:
5884
Concept ID:
C0022013
Molecular Function
4.

Arthritis

Acute or chronic inflammation of JOINTS. [from MeSH]

MedGen UID:
2043
Concept ID:
C0003864
Disease or Syndrome
5.

Rheumatoid arthritis

Inflammatory changes in the synovial membranes and articular structures with widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, as well as atrophy and rarefaction of bony structures. [from HPO]

MedGen UID:
504816
Concept ID:
CN001255
Finding
6.

Mass of body structure

A benign or malignant pathologic structure in any part of the body, resulting from a neoplastic accumulation of cells, inflammatory cells, or cystic changes. [from NCI]

MedGen UID:
108287
Concept ID:
C0577559
Finding
7.

Examined for

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

MedGen UID:
83047
Concept ID:
C0332128
Finding
8.

Van der Woude syndrome

IRF6-related disorders span a spectrum from isolated cleft lip and palate and Van der Woude syndrome (VWS) at the mild end to popliteal pterygium syndrome (PPS) at the more severe end. Individuals with VWS show one or more of the following anomalies: Congenital, usually bilateral, paramedian lower-lip fistulae (pits) or sometimes small mounds with a sinus tract leading from a mucous gland of the lip. Cleft lip (CL). Cleft palate (CP). Note: Cleft lip with or without cleft palate (CL±P) is observed about twice as often as CP only. Submucous cleft palate (SMCP). The PPS phenotype includes the following: CL±P. Fistulae of the lower lip. Webbing of the skin extending from the ischial tuberosities to the heels. In males: bifid scrotum and cryptorchidism. In females: hypoplasia of the labia majora. Syndactyly of fingers and/or toes. Anomalies of the skin around the nails. A characteristic pyramidal fold of skin overlying the nail of the hallux (almost pathognomonic). In some non-classic forms of PPS: filiform synechiae connecting the upper and lower jaws (syngnathia) or the upper and lower eyelids (ankyloblepharon). In both VWS and PPS, growth and intelligence are normal. [from GTR]

MedGen UID:
61233
Concept ID:
C0175697
Disease or Syndrome
9.

Rheumatoid arthritis

Rheumatoid arthritis is an inflammatory disease, primarily of the joints, with autoimmune features and a complex genetic component. [from GTR]

MedGen UID:
2078
Concept ID:
C0003873
Disease or Syndrome
10.

Skin and Connective Tissue Diseases

A collective term for diseases of the skin and its appendages and of connective tissue. [from MeSH]

MedGen UID:
59786
Concept ID:
C0175166
Disease or Syndrome
11.

Polyarticular arthritis

An arthritis affecting five or more separate joints. [from NCI]

MedGen UID:
56408
Concept ID:
C0162323
Disease or Syndrome
12.

Rheumatism

Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. [from MeSH]

MedGen UID:
48447
Concept ID:
C0035435
Disease or Syndrome
13.

Protease preparation

A class of enzymes that catalyze the hydrolysis of peptide bonds in the interior of a polypeptide chain or protein molecule. [from NCI]

MedGen UID:
45389
Concept ID:
C0030946
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
14.

Arthropathy

An abnormal structure or form of the joints, i.e., one or more of the articulations where two bones join. [from HPO]

MedGen UID:
7190
Concept ID:
C0022408
Disease or Syndrome
15.

Autoimmune disease

A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to his own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis). [from NCI]

MedGen UID:
2135
Concept ID:
C0004364
Disease or Syndrome
16.

Connective tissue disorder

A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. [from MeSH]

MedGen UID:
1098
Concept ID:
C0009782
Disease or Syndrome
17.

Synostosis of joints

The abnormal fusion of neighboring bones across a joint. [from HPO]

MedGen UID:
867792
Concept ID:
C4022183
Anatomical Abnormality
18.

CSF chemistry normal

MedGen UID:
614065
Concept ID:
C0438148
Finding
19.

CSF: protein normal

MedGen UID:
606457
Concept ID:
C0428482
Finding
20.

Small and large joint arthritis

MedGen UID:
605555
Concept ID:
C0427310
Finding
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