NM_022369.4(STRA6):c.*582T>C AND Matthew-Wood syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001121004.4
Allele description [Variation Report for NM_022369.4(STRA6):c.*582T>C]
NM_022369.4(STRA6):c.*582T>C
Condition(s)
- Name:
- Matthew-Wood syndrome (MCOPS9)
- Synonyms:
- ANOPHTHALMIA, CLINICAL, WITH MILD FACIAL DYSMORPHISM AND VARIABLE MALFORMATIONS OF THE LUNG, HEART, AND DIAPHRAGM; PULMONARY AGENESIS, MICROPHTHALMIA, AND DIAPHRAGMATIC DEFECT; Microphthalmia syndromic 9; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011010; MedGen: C1832661; Orphanet: 2470; OMIM: 601186
Assertion and evidence details
Last Updated: Jul 29, 2023