NM_000268.4(NF2):c.363+11C>T AND Neurofibromatosis, type 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003023831.2
Allele description [Variation Report for NM_000268.4(NF2):c.363+11C>T]
NM_000268.4(NF2):c.363+11C>T
Condition(s)
- Name:
- Neurofibromatosis, type 2 (SWNV)
- Synonyms:
- NF 2; Neurofibromatosis central type; Acoustic schwannomas bilateral; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007039; MedGen: C0027832; Orphanet: 637; OMIM: 101000
-
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndromeMedGen
-
C4015701[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024