sábado, 24 de marzo de 2018

Lynch syndrome - OMIM - NCBI

Lynch syndrome - OMIM - NCBI

Collage of four individuals living with Lynch Syndrome

From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.





LYNCH SYNDROME II, INCLUDED
Cytogenetic locations: 2p21-p16
2.
PICK COMPLEX, INCLUDED
Cytogenetic locations: 1pter-p36.13, 14q24.2
3.
4.
5.
6.
8.
COLORECTAL CANCER, SUSCEPTIBILITY TO, 4, INCLUDED; CRCS4, INCLUDED
Cytogenetic locations: 15q15.3-q22.1
10.
11.
13.
CAUDAL DYSGENESIS SYNDROME, INCLUDED
Cytogenetic locations: 1p13.1
14.
LYMPHEDEMA-DISTICHIASIS SYNDROME WITH RENAL DISEASE AND DIABETES MELLITUS, INCLUDED
Cytogenetic locations: 16q24.1
17.
Cytogenetic locations: 1pter-p36.13, 2p21-p16
18.
BARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED
Cytogenetic locations: 1p36.13
19.
SACRAL AGENESIS SYNDROME, INCLUDED
Cytogenetic locations: 7q36.3

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