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Items: 6

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.

Position

The anatomical localization of the specified phenotypic abnormality. [from HPO]

MedGen UID:
866377
Concept ID:
C4019252
Spatial Concept
3.

Proboscis

A fleshy, tube-like structure usually located in the midline of the face or just to one side of the midline. [from HPO]

MedGen UID:
786441
Concept ID:
CN188034
Finding
4.

Proboscis

A fleshy, tube-like structure usually located in the midline of the face or just to one side of the midline. [from HPO]

MedGen UID:
673804
Concept ID:
C0687082
Body Part, Organ, or Organ Component
5.

History

The aggregate of past events; the continuum of events occurring in succession leading from the past to the present; a record or narrative description of past events. [from NCI]

MedGen UID:
389153
Concept ID:
C2004062
Finding
6.

History of

A record of a patient's background regarding health and the occurrence of disease events of the individual. In addition, personal medical history may be a variable in epidemiologic studies. [from NCI]

MedGen UID:
82657
Concept ID:
C0262926
Finding
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