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Items: 5

1.

Mitochondrial inheritance

A mode of inheritance that is observed for traits related to a gene encoded on the mitochondrial genome. Because the mitochondrial genome is essentially always maternally inherited, a mitochondrial condition can only be transmitted by females, although the condition can affect both sexes. The proportion of mutant mitochondria can vary (heteroplasmy). [from HPO]

MedGen UID:
165802
Concept ID:
C0887941
Genetic Function
2.

Membrane Fusion

The adherence and merging of cell membranes, intracellular membranes, or artificial membranes to each other or to viruses, parasites, or interstitial particles through a variety of chemical and physical processes. [from MeSH]

MedGen UID:
9952
Concept ID:
C0025246
Molecular Function
3.

Ergosterol

A steroid occurring in FUNGI. Irradiation with ULTRAVIOLET RAYS results in formation of ERGOCALCIFEROL (vitamin D2). [from MeSH]

MedGen UID:
5010
Concept ID:
C0014705
Organic Chemical; Pharmacologic Substance; Vitamin
4.

Mode of inheritance

The pattern in which a particular genetic trait or disorder is passed from one generation to the next. [from HPO]

MedGen UID:
353811
Concept ID:
C1708511
Genetic Function
5.

Lumisterol

MedGen UID:
87659
Concept ID:
C0376173
Organic Chemical; Pharmacologic Substance; Vitamin
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