TMEM38B

transmembrane protein 38B
OMIM: 611236
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Osteogenesis imperfecta, type XIV, OMIM:615066, Osteogenesis imperfecta type 14, MONDO:0014029
R-numbers: R102
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Osteogenesis imperfecta, type XIV, OMIM:615066, Osteogenesis imperfecta type 14, MONDO:0014029
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Osteogenesis imperfecta, type XIV, OMIM:615066, Osteogenesis imperfecta type 14, MONDO:0014029