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Anophthalmia_Microphthalmia_Coloboma v1.5 CDON Zornitza Stark Phenotypes for gene: CDON were changed from Holoprosencephaly 11 MIM#614226 to Coloboma
Anophthalmia_Microphthalmia_Coloboma v0.75 CDON Zornitza Stark Marked gene: CDON as ready
Anophthalmia_Microphthalmia_Coloboma v0.75 CDON Zornitza Stark Gene: cdon has been classified as Amber List (Moderate Evidence).
Anophthalmia_Microphthalmia_Coloboma v0.75 CDON Zornitza Stark Classified gene: CDON as Amber List (moderate evidence)
Anophthalmia_Microphthalmia_Coloboma v0.75 CDON Zornitza Stark Gene: cdon has been classified as Amber List (Moderate Evidence).
Anophthalmia_Microphthalmia_Coloboma v0.74 CDON Elena Savva gene: CDON was added
gene: CDON was added to Anophthalmia_Microphthalmia_Coloboma. Sources: Literature
Mode of inheritance for gene: CDON was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CDON were set to PMID: 32729136
Phenotypes for gene: CDON were set to Holoprosencephaly 11 MIM#614226
Review for gene: CDON was set to AMBER
Added comment: Isolated example of chet (both splice) siblings with isolated coloboma. Parents were normal.
Supported by mouse model.
Reviews a hom patient (PTC) in another case also with retinal coloboma, dev delay, dysmorphic features and an additional hom MAPRE2 variant (gene has not be associated to coloboma)
Sources: Literature