NM_000132.4(F8):c.5950G>C (p.Val1984Leu) AND Hereditary factor VIII deficiency disease
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001001231.8
Allele description [Variation Report for NM_000132.4(F8):c.5950G>C (p.Val1984Leu)]
NM_000132.4(F8):c.5950G>C (p.Val1984Leu)
Condition(s)
- Name:
- Hereditary factor VIII deficiency disease (HEMA)
- Synonyms:
- AUTOSOMAL HEMOPHILIA A; Hemophilia A; Hemophilia A, congenital; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0010602; MedGen: C0019069; Orphanet: 98878; OMIM: 134500; OMIM: 306700
-
Lethal multiple pterygium syndrome
Lethal multiple pterygium syndromeMedGen
-
C1854678[conceptid] (1)
MedGen
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Jun 17, 2024