CBL Results

CBL

Cbl proto-oncogene
04/29/2019

CBLC

Cbl proto-oncogene C

CBLN3

cerebellin 3 precursor

CBLL2

Cbl proto-oncogene like 2

CBLN1

cerebellin 1 precursor

CBLN2

cerebellin 2 precursor

CBLL1

Cbl proto-oncogene like 1

CBLN4

cerebellin 4 precursor

DCBLD1

discoidin, CUB and LCCL domain containing 1

DCBLD2

discoidin, CUB and LCCL domain containing 2

CBLB

Cbl proto-oncogene B

methylmalonic aciduria and homocystinuria type cblC

MONDO_0010184 Condition
Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC
06/29/2020

methylmalonic aciduria and homocystinuria type cblD

MONDO_0010185 Condition
Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD
03/21/2018

vitamin B12-responsive methylmalonic acidemia type cblB

MONDO_0009614 Condition
methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type
03/21/2018

vitamin B12-responsive methylmalonic acidemia type cblA

MONDO_0009613 Condition
methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A type
03/21/2018

vitamin B12-responsive methylmalonic acidemia, type cblDv2

MONDO_0017685 Condition
Vitamin B12-responsive methylmalonic aciduria, type cblDv2

methylcobalamin deficiency type cblE

MONDO_0009354 Condition
Functional methionine synthase deficiency type cblE

methylmalonic acidemia with homocystinuria, type cblJ

MONDO_0013925 Condition
Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblJ

methylcobalamin deficiency type cblG

MONDO_0009609 Condition
Functional methionine synthase deficiency type cblG

methylmalonic aciduria and homocystinuria type cblF

MONDO_0010183 Condition
Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF

methylmalonic acidemia with homocystinuria, type cblX

MONDO_0010657 Condition
Methylmalonic aciduria with homocystinuria, type cblX

methylcobalamin deficiency type cblDv1

MONDO_0017683 Condition
Functional methionine synthase deficiency type cblDv1

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