NM_001199107.2(TBC1D24):c.457G>A (p.Glu153Lys) AND multiple conditions
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Oct 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000850506.8
Allele description [Variation Report for NM_001199107.2(TBC1D24):c.457G>A (p.Glu153Lys)]
NM_001199107.2(TBC1D24):c.457G>A (p.Glu153Lys)
Condition(s)
- Name:
- DOORS syndrome (DOORS)
- Synonyms:
- Deafness onychodystrophy osteodystrophy and mental retardation syndrome; DRC SYNDROME; BRACHYDACTYLY DUE TO ABSENCE OF DISTAL PHALANGES; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009079; MedGen: C0795934; Orphanet: 3231; Orphanet: 79500; OMIM: 220500
- Name:
- Familial infantile myoclonic epilepsy (FIME)
- Synonyms:
- Epilepsy, Myoclonic, Infantile
- Identifiers:
- MONDO: MONDO:0011506; MedGen: C0917800; Orphanet: 352582; OMIM: 605021
- Name:
- Autosomal recessive nonsyndromic hearing loss 86
- Synonyms:
- Deafness, autosomal recessive 86
- Identifiers:
- MONDO: MONDO:0013826; MedGen: C2829265; Orphanet: 90636; OMIM: 614617
Assertion and evidence details
Last Updated: Aug 25, 2024