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Items: 6

3.

#601665 - OBESITY

LEANNESS, INCLUDED

Cytogenetic locations: 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 613602, 1p36, 1p36

4.

#208000 - ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1

CORONARY SCLEROSIS, MEDIAL, OF INFANCY, INCLUDED

Cytogenetic locations: 24196111

6.

#125853 - TYPE 2 DIABETES MELLITUS; T2D

INSULIN RESISTANCE, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, family, KYNUU, 1, in, identified, mutation, 1p36, 1p36, 1p36, 600310, 1p36, 1p36, 1p36, 1, Thrombospondin, 1p36, 1p36, 1p36, 1p36

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