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Items: 1 to 20 of 29

1.

Epidermal growth factor

A protein made by many cells in the body and by some types of tumors. It causes cells to grow and differentiate (become more specialized). It is a type of growth factor and a type of cytokine. [from NCI]

MedGen UID:
66867
Concept ID:
C0242275
Amino Acid, Peptide, or Protein; Hormone; Pharmacologic Substance
2.

Growth delay

A deficiency or slowing down of growth pre- and postnatally. [from HPO]

MedGen UID:
765377
Concept ID:
C3552463
Finding; Sign or Symptom
3.

Intrauterine growth retardation

An abnormal restriction of fetal growth with fetal weight below the tenth percentile for gestational age. [from HPO]

MedGen UID:
473406
Concept ID:
C1386048
Pathologic Function
4.

Growth retardation

Stature that is smaller than normal as expected for age. [from NCI]

MedGen UID:
56240
Concept ID:
C0151686
Pathologic Function
5.

Intrauterine growth restriction

abnormal fetal physical growth or growth potential at any gestational stage. [from CRISP]

MedGen UID:
4693
Concept ID:
C0015934
Pathologic Function
6.

Necrotizing Enterocolitis

ENTEROCOLITIS with extensive ulceration (ULCER) and NECROSIS. It is observed primarily in LOW BIRTH WEIGHT INFANT. [from MeSH]

MedGen UID:
105440
Concept ID:
C0520459
Disease or Syndrome
7.

Enterocolitis

Inflammation of the MUCOSA of both the SMALL INTESTINE and the LARGE INTESTINE. Etiology includes ISCHEMIA, infections, allergic, and immune responses. [from MeSH]

MedGen UID:
4966
Concept ID:
C0014356
Disease or Syndrome
8.

Necrotizing enterocolitis in fetus OR newborn

extensive ulceration and necrosis of the ileum and colon in premature infants in the neonatal period; possibly due to perinatal intestinal ischemia and bacterial invasion. [from CRISP]

MedGen UID:
906305
Concept ID:
C4082937
Disease or Syndrome
9.

Position

The anatomical localization of the specified phenotypic abnormality. [from HPO]

MedGen UID:
866377
Concept ID:
C4019252
Functional Concept
10.

IUGR

MedGen UID:
852391
Concept ID:
CN235083
Finding
11.

Patient currently pregnant

Observed to be or have been pregnant. [from NCI]

MedGen UID:
639841
Concept ID:
C0549206
Finding
12.

Enterocolitis

An inflammation of the colon and small intestine. However, most conditions are either categorized as Enteritis (inflammation of the small intestine) or Colitis (inflammation of the large intestine). [from HPO]

MedGen UID:
505618
Concept ID:
CN003886
Finding
13.

PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY

MedGen UID:
349287
Concept ID:
C1861457
Disease or Syndrome
14.

Proliferation

Growth and reproduction of new similar forms, e.g. cells, buds, or offspring. [from NCI]

MedGen UID:
137720
Concept ID:
C0334094
Functional Concept; Pathologic Function
15.

Feeding difficulties

Impaired ability to eat related to problems gathering food and getting ready to suck, chew, or swallow it. [from HPO]

MedGen UID:
65429
Concept ID:
C0232466
Finding
16.

Female Urogenital Diseases and Pregnancy Complications

Pathological processes of the female URINARY TRACT, the reproductive system (GENITALIA, FEMALE), and disorders related to PREGNANCY. [from MeSH]

MedGen UID:
318565
Concept ID:
C1720765
Disease or Syndrome
17.

Pregnancy Complications

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
18.

Embryopathies

MedGen UID:
41754
Concept ID:
C0013949
Disease or Syndrome
19.

Clinical finding

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

MedGen UID:
19974
Concept ID:
C0037088
Sign or Symptom
20.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Diseases existing at birth and often before birth, or that develop during the first month of life (INFANT, NEWBORN, DISEASES), regardless of causation. Of these diseases, those characterized by structural deformities are termed CONGENITAL ABNORMALITIES. [from MeSH]

MedGen UID:
14319
Concept ID:
C0027612
Congenital Abnormality; Disease or Syndrome
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