Update History
Condition: Biotinidase Deficiency
Gene/Gene Panel: BTD
Context: Adult
2024/03/24
Released
1.2.5
Morbidity and mortality from biotin deficiency
(GroupA)
Referral to a metabolic specialist for evaluation and biotin supplementation
(GroupA)
6DC
System migration to fix the sem versioning
Assertions
Gene Condition Pairs
Suggested Assertion
Final Assertion
BTD
⇔
0009665 BIOTINIDASE DEFICIENCY
Limited Actionability
Limited Actionability
2024/03/24
Released
(Under revision)
Morbidity and mortality from biotin deficiency
(GroupA)
Referral to a metabolic specialist for evaluation and biotin supplementation
(GroupA)
6DC
Assertions
Gene Condition Pairs
Suggested Assertion
Final Assertion
BTD
⇔
0009665 BIOTINIDASE DEFICIENCY
Limited Actionability
Limited Actionability
2022/10/03
Released
Morbidity and mortality from biotin deficiency
(GroupA)
Referral to a metabolic specialist for evaluation and biotin supplementation
(GroupA)
6DC
Assertions
Gene Condition Pairs
Suggested Assertion
Final Assertion
BTD
⇔
0009665 BIOTINIDASE DEFICIENCY
Limited Actionability
Limited Actionability
2022/08/31
Released
(Under revision)
1.2.3
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
Internal system migration associated with MONDO name addition.
2022/02/09
Released
1.2.3
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
Internal system migration associated with MONDO name addition.
2022/02/09
Released
(Under revision)
1.2.2
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
2020/04/29
Released
1.2.2
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
2020/04/29
Released
(Under revision)
1.2.1
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
Updated to include a link to the ACMG ACT Sheet. Other parts of the report not updated.
2020/01/31
Released
1.2.1
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
Updated to include a link to the ACMG ACT Sheet. Other parts of the report not updated.
2020/01/31
Released
(Under revision)
1.2.0
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
Internal system migration associated with Gene-Disease scoring groups upgrades.
2019/10/03
Released
1.2.0
Cutaneous manifestations
(GroupA)
Biotin therapy
(GroupA)
10CC
Neurological complications
(GroupA)
Biotin therapy
(GroupA)
11CC
Internal system migration associated with Gene-Disease scoring groups upgrades.
2019/04/04
Released
1.1.0
Cutaneous manifestations
Biotin therapy
10CC
Neurological complications
Biotin therapy
11CC
Internal system migration related to merging adult and pediatric contexts.
2018/11/01
Released
1.0.2
Cutaneous manifestations
Biotin therapy
10CC
Neurological complications
Biotin therapy
11CC
Internal system migration related to score text replacement from E to N
2018/01/11
Released
1.0.1
Cutaneous manifestations
Biotin therapy
10CC
Neurological complications
Biotin therapy
11CC
2017/10/23
Released
1.0.0
Cutaneous manifestations
Biotin therapy
10CC
Neurological complications
Biotin therapy
11CC