|
phthioceranic acid
|
C522296 |
|
|
centrin3 protein, Trypanosoma brucei brucei
|
C000601660 |
|
|
Biological Coevolution
|
D000073930 |
[The process of reciprocal evolutionary change occurring between pairs of species or among groups of species as they interact.
] |
|
fasciospongine A
|
C522297 |
|
|
Adverse Outcome Pathways
|
D000073931 |
[Models connecting initiating events at the cellular and molecular level to population-wide impacts. Computational models may be at levels relating toxicology to adverse effects.
] |
|
fasciospongine B
|
C522298 |
|
|
Food Addiction
|
D000073932 |
[A cluster of chemical dependencies to specific foods or food in general in which there develops a physical craving for these foods.
] |
|
Narrative Medicine
|
D000073935 |
[NARRATION as a tool to collect and interpret information on a patient's experience of illness
] |
|
Risk Evaluation and Mitigation
|
D000073938 |
[Strategies required by the US Food and Drug Administration (FDA) Amendments Act of 2007 when a question exists as to whether the benefits of a drug outweigh its risks. These constitute a safety plan with several potential components, including a medication guide, a communication plan, elements to ensure safe use and an implementation system to help guide the prescribers, pharmacists and patients.
] |
|
NSC13345
|
C000601669 |
|
|
Dysferlin
|
D000073939 |
[A membrane protein that contains multiple C2 DOMAINS. It is highly expressed in skeletal muscle and functions as a calcium ion sensor in SYNAPTIC VESICLE-PLASMA MEMBRANE fusion, as well as in SARCOLEMMA repair following mechanical stress. Mutations in the dysferlin (DYSF) gene are associated with several hereditary MUSCULAR DYSTROPHIES.
] |
|
COG8 protein, human
|
C522290 |
|
|
Distal myopathy, Nonaka type
|
C536816 |
|
|
Al-Gazali Syndrome
|
C536817 |
|
|
Giant mammary hamartoma
|
C536818 |
|
|
Melanocytic nevus syndrome, congenital
|
C536819 |
|
|
Chromosome 3, monosomy 3q27
|
C536810 |
|
|
Chromosome 3, trisomy 3p
|
C536811 |
|
|
Chromosome 3, trisomy 3p25
|
C536812 |
|
|
Chromosome 3, trisomy 3q
|
C536813 |
|
