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Results: 1 to 20 of 39

1.

Mutant

An altered form of an individual, organism, population, or genetic character that differs from the corresponding wild type due to one or more alterations (mutations). [from NCI]

MedGen UID:
109303
Concept ID:
C0596988
Cell or Molecular Dysfunction
2.

Fiber

An elongated, tapering, generally thick-walled sclerenchyma cell of vascular plants; its walls may or may not be lignified. [from NCI]

MedGen UID:
68338
Concept ID:
C0225326
Pharmacologic Substance
3.

Complete deafness

MedGen UID:
108418
Concept ID:
C0581883
Finding
4.

Deafness

A general term for the complete loss of the ability to hear from both ears. [from MeSH]

MedGen UID:
4155
Concept ID:
C0011053
Finding
5.

Absence

MedGen UID:
739164
Concept ID:
C1689985
Anatomical Abnormality
6.

Profound

MedGen UID:
615266
Concept ID:
C0439808
7.

Error occurred: cannot get document summary

ID:
449087

8.

Hearing impairment

A `decreased magnitude` (PATO:0002018) of the `sensory perception of sound` (GO:0007605). [from HPO]

MedGen UID:
446352
Concept ID:
CN000341
Finding
9.

Severe

A term used to describe cells that look abnormal under a microscope. These cells are more likely to grow and spread quickly than cells in low-grade cancer or in growths that may become cancer. [from NCI]

MedGen UID:
104640
Concept ID:
C0205082
10.

Congenital deafness

complete loss of the ability to hear from both ears since birth, regardless of causation. [from CRISP]

MedGen UID:
83296
Concept ID:
C0339789
Disease or Syndrome
11.

Tissue Degeneration

MedGen UID:
3705
Concept ID:
C0011164
Pathologic Function
12.

Dysacusis

MedGen UID:
267601
Concept ID:
C1510450
Sign or Symptom
13.

hearing impairment

A general term for the complete or partial loss of the ability to hear from one or both ears. [from MeSH]

MedGen UID:
235586
Concept ID:
C1384666
Finding
14.

Deafness, Acquired

MedGen UID:
196717
Concept ID:
C0751068
Disease or Syndrome
15.

Murine

MedGen UID:
108834
Concept ID:
C0591833
Pharmacologic Substance
16.

Hearing problem

Conditions that impair the transmission of auditory impulses and information from the level of the ear to the temporal cortices, including the sensorineural pathways. [from MeSH]

MedGen UID:
82636
Concept ID:
C0260662
Disease or Syndrome
17.

Paracusis

Altered sense of hearing, other than simple decreased hearing or deafness [from SNOMED CT]

MedGen UID:
57838
Concept ID:
C0155536
Sign or Symptom
18.

Pathological Conditions, Signs and Symptoms

Abnormal anatomical or physiological conditions and objective or subjective manifestations of disease, not classified as disease or syndrome. [from MeSH]

MedGen UID:
21047
Concept ID:
C0039058
Sign or Symptom
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.

Sensation Disorders

Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM). [from MeSH]

MedGen UID:
19934
Concept ID:
C0036659
Disease or Syndrome

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