Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Antibody absorption, red blood cell, cold with autoabsorption (procedure) | 35435005 | |
| Under care of research nurse (finding) | 305585002 | |
| Laparoscopic anastomosis of gallbladder to intestine (procedure) | 440581009 | |
| 937.5 (qualifier value) | 769347008 | |
| Agar dental impression material (physical object) | 468248002 | |
| Repair of acquired femoral arteriovenous fistula (procedure) | 699070001 | |
| Repair of congenital femoral arteriovenous fistula (procedure) | 709094003 | |
| Souffle cheese (substance) | 227649002 | |
| Spondyloepimetaphyseal dysplasia Missouri type (disorder) | 719171005 | [Disorder with manifestations of moderate-to-severe metaphyseal changes, mild epiphyseal involvement, rhizomelic shortening of the lower limbs with bowing of the femora and/or tibiae, coxa vara, genu varum and pear-shaped vertebrae in childhood. The syndrome has been described in a large Missouri (US) kindred with 14 affected members in 4 generations. Though some spontaneous improvement of the skeletal defects may occur in adolescence, the affected individuals remained shorter than their age-matched unaffected siblings. Predisposition deformities to osteoarthritis have been noted. This condition is caused by mutation in the MMP13 gene (locus 11q22.3) and transmitted in an autosomal dominant manner.] |
| Rivermead behavioral memory test - adult version (assessment scale) | 307801002 | |
| Infection caused by Paragonimus kellicotti (disorder) | 75256000 | |
| Hypohidrosis of unknown etiology (disorder) | 723150006 | |
| Product containing only phenylephrine in cutaneous dose form (medicinal product form) | 780199004 | |
| Prurigo nodularis (disorder) | 63501000 | |
| Blood group antigen WH (substance) | 115874001 | |
| Eimeria striata (organism) | 52133008 | |
| Smoked before confirmation of pregnancy (finding) | 449345000 | |
| Strain M 84 (qualifier value) | 261924009 | |
| White forelock with malformations syndrome (disorder) | 763619009 | [A multiple congenital anomalies syndrome with characteristics of poliosis, distinct facial features (epicanthal folds, hypertelorism, posterior rotation of ears, prominent philtrum, high-arched palate) and congenital anomalies/malformations of the eye (blue sclera), cardiopulmonary (atrial septal defect, prominent thoracic and abdominal veins) and skeletal (clinodactyly, syndactyly of the fingers and second and third toes) systems. There have been no further descriptions in the literature since 1980.] |
| Poliosis (disorder) | 14240001 |