| CAHMR | cataract-hypertrichosis-mental retardation [syndrome] |
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| HL | hairline; hairy leukoplakia; half life; hearing level; hearing loss; heparin lock; histiocytic lymph... |
| SAHA | seborrhea-hypertrichosis/hirsutism-alopecia [syndrome] |
| UHL | universal hypertrichosis lanuginosa |
| MNBCCS | multiple nevoid basal-cell carcinoma syndrome |
| NBCCS | Nevoid Basal Cell Carcinoma Syndrome |
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| nevoid hypertrichosis | Congenital growth of hair abnormal for its site, texture, colour, or length; often associated with other nevoid abnormalities. (05 Mar 2000) |
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| hypertrichosis | Excessive growth of the hair. Also called polytrichia and polytrichosis. (cf. Hirsutism) Origin: Gr. Thrix = hair (18 Nov 1997) |
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| hypertrichosis lanuginosa | Excessive growth of lanugo hair associated with internal malignancy. (05 Mar 2000) |
| hypertrichosis partialis | Abnormally excessive hair growth in patches in unusual areas. (05 Mar 2000) |
| hypertrichosis universalis | Generalised excessive hair growth. (05 Mar 2000) |
| nevoid | Resembling a nevus. Synonym: nevose, nevous. Origin: L. Naevus, mole (nevus), + G. Eidos, resemblance (05 Mar 2000) |
| nevoid amentia | A familial disorder characterised by unilateral nevus, contralateral hemiplegia, hemianopia, cerebral angioma, and mental retardation; possibly a variant of Sturge-Weber syndrome. Synonym: nevoid amentia. (05 Mar 2000) |
| nevoid basal cell carcinoma syndrome | <syndrome> An inherited group of defects which involve abnormalities of the skin, eyes, nervous system, endocrine, glands and bones. The condition is characterised by an unusual facial appearance and a predisposition for skin cancer. (27 Sep 1997) |
| nevoid elephantiasis | Thickening of skin, usually unilateral, involving a small area or the entire extremity, due to congenital enlargement of lymph vessels and lymph vessel obstruction. (05 Mar 2000) |
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