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Amygdala
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A08.186.211.180.090 |
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Infection Control, Dental
|
N06.850.780.200.450.500 |
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Ichthyosiform Erythroderma, Congenital
|
D016113 |
[Designation for several severe forms of ichthyosis, present at birth, that are characterized by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalized scaling. The forms include bullous (HYPERKERATOSIS, EPIDERMOLYTIC), non-bullous (ICHTHYOSIS, LAMELLAR), wet type, and dry type.
] |
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Geotrichum
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B01.300.381.380 |
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Ichthyosis, X-Linked
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D016114 |
[Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the X-chromosome and transmitted to the male offspring. It is characterized by severe scaling, especially on the extremities, and is associated with steroid sulfatase deficiency.
] |
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Sjogren-Larsson Syndrome
|
D016111 |
[An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism.
] |
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Wolfram Syndrome
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C10.597.751.418.341.186.500.750 |
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Ichthyosis Vulgaris
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D016112 |
[Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.
] |
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Albinism, Ocular
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D016117 |
[Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity.
] |
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Cabo Verde
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D055726 |
[A country in western Africa composed of a group of islands in the North Atlantic Ocean, west of Senegal. The capital is Praia.
] |
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Anterior Cruciate Ligament
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D016118 |
[A strong ligament of the knee that originates from the posteromedial portion of the lateral condyle of the femur, passes anteriorly and inferiorly between the condyles, and attaches to the depression in front of the intercondylar eminence of the tibia.
] |
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Albinism, Oculocutaneous
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D016115 |
[Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.
] |
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Electrophysiological Phenomena
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D055724 |
[The electrical properties, characteristics of living organisms, and the processes of organisms or their parts that are involved in generating and responding to electricity.
] |
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Piebaldism
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D016116 |
[Autosomal dominant, congenital disorder characterized by localized hypomelanosis of the skin and hair. The most familiar feature is a white forelock presenting in 80 to 90 percent of the patients. The underlying defect is possibly related to the differentiation and migration of melanoblasts, as well as to defective development of the neural crest (neurocristopathy). Piebaldism may be closely related to WAARDENBURG SYNDROME.
] |
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Transfer RNA Aminoacylation
|
G02.111.660.050.860 |
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Aminoacylation
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G02.111.660.050 |
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Lymphocyte Subsets
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D016131 |
[A classification of lymphocytes based on structurally or functionally different populations of cells.
] |
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Immunophenotyping
|
D016130 |
[Process of classifying cells of the immune system based on structural and functional differences. The process is commonly used to analyze and sort T-lymphocytes into subsets based on CD antigens by the technique of flow cytometry.
] |
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Armillaria
|
B01.300.179.100.125 |
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GTP-Binding Protein alpha Subunits, Gq-G11
|
D12.776.543.325.100.300 |
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