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Items: 1 to 20 of 35

1.

Hydrops fetalis

A condition characterized by fluid accumulation in two or more anatomic compartments in the fetus.(NICHD) [from NCI]

MedGen UID:
6947
Concept ID:
C0020305
Disease or Syndrome
2.

Anemia

A reduction in erythrocytes volume or hemoglobin concentration. [from HPO]

MedGen UID:
1526
Concept ID:
C0002871
Disease or Syndrome
3.

Hydrops fetalis

The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. [from HPO]

MedGen UID:
504951
Concept ID:
CN001623
Finding
4.

Absent thumb

Absent thumb, i.e., the absence of both phalanges of a thumb and the associated soft tissues. [from HPO]

MedGen UID:
480441
Concept ID:
C3278811
Congenital Abnormality; Finding
5.

Congenital anemia

Anemia, the cause of which is present at birth. [from NCI]

MedGen UID:
102361
Concept ID:
C0158995
Disease or Syndrome
6.

Immune

Protected against infectious disease by either specific or non-specific mechanisms.(On-line Medical Dictionary) [from NCI]

MedGen UID:
98553
Concept ID:
C0439662
Finding
7.

Anemia

A laboratory test result demonstrating decreased levels of hemoglobin in a biological specimen. [from NCI]

MedGen UID:
56401
Concept ID:
C0162119
Finding
8.

Edema

Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. [from MeSH]

MedGen UID:
4451
Concept ID:
C0013604
Sign or Symptom
9.

Severe

Having a high degree of severity. For quantitative traits, a deviation of between four and five standard deviations from the appropriate population mean. [from HPO]

MedGen UID:
104640
Concept ID:
C0205082
Qualitative Concept
10.

Anasarca

A condition that is characterized by the presence of generalized edema. Causes include congestive heart failure, liver failure, renal failure, and severe malnutrition. [from NCI]

MedGen UID:
101794
Concept ID:
C0151603
Pathologic Function
11.

Pregnancy Complication

The co-occurrence of pregnancy and a disease. The disease may precede or follow conception and it may or may not have a deleterious effect on the pregnant woman or fetus. [from NCI]

MedGen UID:
46066
Concept ID:
C0032962
Disease or Syndrome
12.

Hemoglobinopathy

A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. [from MeSH]

MedGen UID:
42400
Concept ID:
C0019045
Disease or Syndrome
13.

Embryopathies

MedGen UID:
41754
Concept ID:
C0013949
Disease or Syndrome
14.

Thalassemia

A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. [from MeSH]

MedGen UID:
21121
Concept ID:
C0039730
Disease or Syndrome
15.

Clinical finding

Clinical manifestations that can be either objective when observed by a physician, or subjective when perceived by the patient. [from MeSH]

MedGen UID:
19974
Concept ID:
C0037088
Sign or Symptom
16.

Syndrome

A characteristic symptom complex. [from MeSH]

MedGen UID:
11688
Concept ID:
C0039082
Disease or Syndrome
17.

Fetal disorder

A non-neoplastic or neoplastic disorder which occurs in the fetus. [from NCI]

MedGen UID:
8822
Concept ID:
C0015929
Disease or Syndrome
18.

Multiple congenital anomalies

Congenital abnormalities that affect more than one organ or body structure. [from MeSH]

MedGen UID:
7806
Concept ID:
C0000772
Congenital Abnormality
19.

Hemic and Lymphatic Diseases

Hematologic diseases and diseases of the lymphatic system collectively. Hemic diseases include disorders involving the formed elements (e.g., ERYTHROCYTE AGGREGATION, INTRAVASCULAR) and chemical components (e.g., BLOOD PROTEIN DISORDERS); lymphatic diseases include disorders relating to lymph, lymph nodes, and lymphocytes. [from MeSH]

MedGen UID:
6780
Concept ID:
C0018981
Disease or Syndrome
20.

Hematologic disease

An abnormality of the hematopoietic system. [from HPO]

MedGen UID:
5483
Concept ID:
C0018939
Disease or Syndrome
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