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- The CAC Wirraway is a training and general purpose military aircraft manufactured in Australia by the Commonwealth Aircraft Corporation (CAC) between 1939...44 KB (5,555 words) - 00:17, 10 September 2024
- Astaxanthin /æstəˈzænθɪn/ is a keto-carotenoid within a group of chemical compounds known as carotenones or terpenes. Astaxanthin is a metabolite of zeaxanthin...28 KB (2,640 words) - 05:08, 22 August 2024
- Oguchi disease is an autosomal recessive form of congenital stationary night blindness associated with fundus discoloration and abnormally slow dark adaptation...5 KB (483 words) - 01:55, 9 June 2023
- Werner syndrome (WS) or Werner's syndrome, also known as "adult progeria", is a rare, autosomal recessive disorder which is characterized by the appearance...36 KB (4,516 words) - 08:24, 12 September 2024
- The HAL Light Utility Helicopter (LUH), along with its derivative, Light Observation Helicopter (LOH), was designed and developed by the Rotary Wing Research...36 KB (2,950 words) - 05:49, 13 September 2024
- 45,X/46,XY mosaicism, also known as X0/XY mosaicism and mixed gonadal dysgenesis, is a mutation of sex development in humans associated with sex chromosome...9 KB (1,048 words) - 17:47, 1 August 2024
- Gonadal dysgenesis is classified as any congenital developmental disorder of the reproductive system characterized by a progressive loss of primordial...23 KB (2,160 words) - 12:08, 2 August 2024
- Traceability is the capability to trace something. In some cases, it is interpreted as the ability to verify the history, location, or application of an...22 KB (2,581 words) - 20:37, 20 February 2024
- Aplasia cutis congenita is a rare disorder characterized by congenital absence of skin. Ilona J. Frieden classified ACC in 1986 into 9 groups on the basis...5 KB (519 words) - 04:50, 5 May 2024
- Triosephosphate isomerase deficiency is a rare autosomal recessive metabolic disorder which was initially described in 1965. It is a unique glycolytic...5 KB (424 words) - 14:46, 6 March 2023
- Upington disease is an extremely rare autosomal dominant malformation disorder. It has only one published source claiming its existence in three generations...3 KB (200 words) - 23:03, 6 November 2023
- Rothmund–Thomson syndrome (RTS) is a rare autosomal recessive skin condition. There have been several reported cases associated with osteosarcoma. A hereditary...10 KB (914 words) - 19:56, 23 August 2024
- Munin is a free and open-source computer system monitoring, network monitoring, and infrastructure monitoring software application. Munin is written in...5 KB (377 words) - 19:06, 8 May 2024
- Urocanic aciduria is an autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase. It is a secondary disorder of histidine...4 KB (301 words) - 00:59, 25 April 2022
- Sarcosinemia (SAR), also called hypersarcosinemia and SARDH deficiency, is a rare autosomal recessive metabolic disorder characterized by an increased...3 KB (278 words) - 07:12, 11 March 2023
- Zaspopathy, also called ZASP-related myofibril myopathy, is a novel autosomal dominant form of progressive muscular dystrophy, first described in 2005...3 KB (224 words) - 14:03, 18 August 2022
- Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal...3 KB (259 words) - 19:56, 23 August 2024
- Sakati–Nyhan–Tisdale syndrome, is a rare genetic disorder that has been associated with abnormalities in the bones of the legs, congenital heart defects...5 KB (360 words) - 16:09, 9 October 2023
- Breast cancer management takes different approaches depending on physical and biological characteristics of the disease, as well as the age, over-all health...53 KB (6,748 words) - 01:23, 10 February 2024
- Opsismodysplasia is a type of skeletal dysplasia (a bone disease that interferes with bone development) first described by Zonana and associates in 1977...11 KB (1,107 words) - 13:42, 8 October 2021