|
Chromosomes, Human, Pair 11
|
D002880 |
[A specific pair of GROUP C CHROMOSOMES of the human chromosome classification.
] |
|
Chromosomes, Human, Pair 12
|
D002881 |
[A specific pair of GROUP C CHROMOSOMES of the human chromosome classification.
] |
|
Immunoglobulin Light Chains, Surrogate
|
D12.776.124.790.651.705.750.775 |
|
|
Chromosomes, Human, Pair 15
|
D002884 |
[A specific pair of GROUP D CHROMOSOMES of the human chromosome classification.
] |
|
Chromosomes, Human, Pair 16
|
D002885 |
[A specific pair of GROUP E CHROMOSOMES of the human chromosome classification.
] |
|
Single-Parent Family
|
I01.880.853.150.750 |
|
|
Chromosomes, Human, Pair 13
|
D002882 |
[A specific pair of GROUP D CHROMOSOMES of the human chromosome classification.
] |
|
Health Status
|
N06.850.505.400.425 |
|
|
Chromosomes, Human, Pair 14
|
D002883 |
[A specific pair of GROUP D CHROMOSOMES of the human chromosome classification.
] |
|
Rh Isoimmunization
|
D012203 |
[The process by which fetal Rh+ erythrocytes enter the circulation of an Rh- mother, causing her to produce IMMUNOGLOBULIN G antibodies, which can cross the placenta and destroy the erythrocytes of Rh+ fetuses. Rh isoimmunization can also be caused by BLOOD TRANSFUSION with mismatched blood.
] |
|
N-Terminal Acetyltransferase D
|
D08.811.913.050.134.423.400 |
|
|
Rh-Hr Blood-Group System
|
D012204 |
[Erythrocyte isoantigens of the Rh (Rhesus) blood group system, the most complex of all human blood groups. The major antigen Rh or D is the most common cause of erythroblastosis fetalis.
] |
|
Ustekinumab
|
D12.776.124.790.651.114.224.060.937 |
|
|
Tyrphostins
|
D02.626.886 |
|
|
Rhabdiasoidea
|
D012205 |
[A superfamily of intestinal nematode parasites containing one genus, STRONGYLOIDES, and several species. It is transmitted through fecal material onto the skin and occurs in animals and humans.
] |
|
Reticuloendotheliosis virus
|
B04.613.807.375.700.700 |
|
|
Rhabdomyolysis
|
D012206 |
[Necrosis or disintegration of skeletal muscle often followed by myoglobinuria.
] |
|
Rhabdomyoma
|
D012207 |
[A benign tumor derived from striated muscle. It is extremely rare, generally occurring in the tongue, neck muscles, larynx, uvula, nasal cavity, axilla, vulva, and heart. These tumors are treated by simple excision. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1354)
] |
|
Rhabdomyosarcoma
|
D012208 |
[A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9)
] |
|
Desmocollins
|
D12.776.543.550.200.200.500.249 |
|
