MED12

mediator complex subunit 12
OMIM: 300188
PanelMode of inheritanceDetails
6 panels
R-numbers: R83
Signed-off version 4.1
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
MED12-related disorders, Opitz-Kaveggia syndrome, OMIM:305450, Ohdo syndrome, X-linked, OMIM:300895, Lujan-Fryns syndrome, OMIM:309520
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
OPITZ-KAVEGGIA SYNDROME 305450, LUJAN-FRYNS SYNDROME 309520
R-numbers: R21, R412
Signed-off version 2.4
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
LUJAN-FRYNS SYNDROME, OPITZ-KAVEGGIA SYNDROME
R-numbers: R59
Signed-off version 3.1
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Lujan-Fryns syndrome, 309520, Opitz-Kaveggia syndrome, 305450
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Opitz-Kaveggia syndrome, 305450, Lujan-Fryns syndrome, 309520, Ohdo syndrome, X-linked, 300895, OPITZ-KAVEGGIA SYNDROME (OKS)
R-numbers: R32
Signed-off version 3.3
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Hardikar syndrome, OMIM:612726, cholestasis-pigmentary retinopathy-cleft palate syndrome, MONDO:0012997