sábado, 24 de noviembre de 2018

Family health history - OMIM - NCBI

Family health history - OMIM - NCBI

a multigenerational family

From NIH OMIM

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



CYCLIC VOMITING SYNDROME WITH NEUROMUSCULAR DISEASE, INCLUDED
2.
PANCREATIC COLIPASE DEFICIENCY, INCLUDED
Cytogenetic locations: 10q25.3
5.
PON1 ENZYME ACTIVITY, VARIATION IN, INCLUDED
Cytogenetic locations: 7q21.3
6.
ANGIOSTATIN, INCLUDED
Cytogenetic locations: 6q26
7.
8.
9.
PTEN HAMARTOMA TUMOR SYNDROME, INCLUDED; PHTS, INCLUDED
Cytogenetic locations: 10q23.31
10.
11.
ANGIOTENSIN I-CONVERTING ENZYME, PLASMA LEVEL OF, INCLUDED
Cytogenetic locations: 17q23.3
12.
13.
14.
16.
19.
20.

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