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Hydrops fetalis v1.0 THSD1 Gene migrated from ENSG00000136114 to ENSG00000136114 (gene set migration)
Hydrops fetalis v0.295 THSD1 Zornitza Stark Phenotypes for gene: THSD1 were changed from Hydrops fetalis MONDO:0015193, THSD1-related to Lymphatic malformation 13, MIM# 620244
Hydrops fetalis v0.294 THSD1 Zornitza Stark reviewed gene: THSD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Lymphatic malformation 13, MIM# 620244; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hydrops fetalis v0.282 THSD1 Zornitza Stark Classified gene: THSD1 as Green List (high evidence)
Hydrops fetalis v0.282 THSD1 Zornitza Stark Gene: thsd1 has been classified as Green List (High Evidence).
Hydrops fetalis v0.281 THSD1 Zornitza Stark Marked gene: THSD1 as ready
Hydrops fetalis v0.281 THSD1 Zornitza Stark Gene: thsd1 has been classified as Amber List (Moderate Evidence).
Hydrops fetalis v0.281 THSD1 Zornitza Stark Phenotypes for gene: THSD1 were changed from nonimmune hydrops fetalis to Hydrops fetalis MONDO:0015193, THSD1-related
Hydrops fetalis v0.280 THSD1 Elena Savva Classified gene: THSD1 as Amber List (moderate evidence)
Hydrops fetalis v0.280 THSD1 Elena Savva Gene: thsd1 has been classified as Amber List (Moderate Evidence).
Hydrops fetalis v0.279 THSD1 Elena Savva gene: THSD1 was added
gene: THSD1 was added to Hydrops fetalis. Sources: Literature
Mode of inheritance for gene: THSD1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: THSD1 were set to PMID: 33569873; 27895300
Phenotypes for gene: THSD1 were set to nonimmune hydrops fetalis
Review for gene: THSD1 was set to GREEN
Added comment: PMID: 33569873 - 1 fetus with a homozygous PTC and nonimmune hydrops fetalis (NIHF), congenital heart disease and hemangiomas. Mother described as having Crohns disease but nothing else unusual, no comments on the father. Fx of 1/3 triplets with severe hydrops fetalis, not sequenced.
- Paper reviews previous NIHF cases and reports another homozygous PTC in two families (4, 2 affected) and a recurring homozygous missense (p.Cys206Tyr) in three families (6, 4, 3 affected).
- No mention of clinically affected heterozygotes.

PMID: 27895300- Mouse model has hydrocephaly with poor perfusion.
Sources: Literature