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Items: 4

1.

Major affective disorder 2

MedGen UID:
326975
Concept ID:
C1839839
Mental or Behavioral Dysfunction
2.

X-linked inheritance

A mode of inheritance that is observed for traits related to a gene encoded on the X chromosome. [from HPO]

MedGen UID:
66838
Concept ID:
C0241764
Genetic Function
3.

Muscular dystrophy

The term dystrophy means abnormal growth. However, muscular dystrophy is used to describe primary myopathies with a genetic basis and a progressive course characterized by progressive skeletal muscle weakness and wasting, defects in muscle proteins, and histological features of muscle fiber degeneration (necrosis) and regeneration. If possible, it is preferred to use other HPO terms to describe the precise phenotypic abnormalities. [from HPO]

MedGen UID:
44527
Concept ID:
C0026850
Disease or Syndrome
4.

Renal phenotype

MedGen UID:
833944
Concept ID:
CN230747
Finding
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