TENM3

teneurin transmembrane protein 3
OMIM: 610083
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, syndromic 15, OMIM:615145, ?Microphthalmia, isolated, with coloboma 9, OMIM:615145, Microphthalmia, isolated, with coloboma 9, MONDO:0014059
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, syndromic 15, OMIM:615145, ?Microphthalmia, isolated, with coloboma 9, OMIM:615145, Microphthalmia, isolated, with coloboma 9, MONDO:0014059
R-numbers: R36
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, syndromic 15, OMIM:615145, ?Microphthalmia, isolated, with coloboma 9, OMIM:615145, Microphthalmia, isolated, with coloboma 9, MONDO:0014059