| SHP | Schonlein-Henoch purpura; secondary hyperparathyroidism; state health plan |
|---|---|
| SHPDA | State Health Planning and Development Agency |
| sHPT | secondary hyperparathyroidism |
| SHP | Scholein-Henoch purpura |
|---|---|
| SHP | Summer-type hypersensitivity pneumonitis |
| SHPT | secondary hyperparathyroidism |
| ShpI metalloprotease | <enzyme> Extracellular neutral metalloprotease from staphylococcus hyicus subsp. Hyicus; contains zn; low substrate specificity; genbank x73315 Registry number: EC 3.4.24.- (26 Jun 1999) |
|---|---|
| ShpII metalloprotease | <enzyme> A 34 kD metalloprotease from staphylococcus hyicus involved in extracellular lipase processing; amino acid sequence has been determined Registry number: EC 3.4.24.- (26 Jun 1999) |
| shprintzen syndrome | <syndrome> Congenital malformation (birth defect) syndrome with cleft palate, heart defect, abnormal face, and learning problems. The condition is also called the velo-cardio-facial (vcf) syndrome. (the velum is the soft palate). Other less frequent features include short stature, small-than-normal head (microcephaly), mental retardation, minor ear anomalies, slender hands and digits, and inguinal hernia. The cause is usually a microdeletion in chromosome band 22q11.2, just as in digeorge syndrome. Shprintzen and digeorge syndromes are different clinical expressions of essentially the same chromosome defect. (12 Dec 1998) |
Synonyms : Haematopoietic Cell Phosphatase, Hematopoietic Cell Phosphatase, Hematopoietic Cell-Specific Tyrosine Phosphatase SHP-1, Protein Tyrosine Phosphatase 1C, Protein Tyrosine Phosphatase, Nonreceptor Type 6, SHP-1 Phosphatase, SHP-1 Protein-Tyrosine Phosphatase
| Shprintzen's s. |
velocardiofacial s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| Shprintzen's syndrome |
see velocardiofacial syndrome, under syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|