NM_000325.6(PITX2):c.*373GTT[1] AND Cataract
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000297372.6
Allele description [Variation Report for NM_000325.6(PITX2):c.*373GTT[1]]
NM_000325.6(PITX2):c.*373GTT[1]
Condition(s)
- Name:
- Cataract
- Synonyms:
- Cataract (disease)
- Identifiers:
- MONDO: MONDO:0005129; MeSH: D002386; MedGen: C0086543; OMIM: PS116200; Human Phenotype Ontology: HP:0000518
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Rhamdia aff. quelen Per1 isolate PeruU01 cardiac muscle myosin heavy chain 6 alpha (myh6) gene, partial cdsgi|1861718351|gb|MT469518.1|Nucleotide
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Dirioxa pornia bio-material BQ85 cytochrome oxidase subunit I (COI) gene, partia...
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hypothetical protein HMPREF1006_02830 [Synergistes sp. 3_1_syn1]
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Last Updated: May 1, 2024