Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Ehlers Danlos syndrome with a likely monogenic cause v2.40 RIN2 Ivone Leong Added comment: Comment on phenotypes: Previous phenotypes:
Macrocephaly, alopecia, cutis laxa, and scoliosis, 613075;RIN2 syndrome;MACS syndrome
Ehlers Danlos syndrome with a likely monogenic cause v2.40 RIN2 Ivone Leong Phenotypes for gene: RIN2 were changed from Macrocephaly, alopecia, cutis laxa, and scoliosis, 613075; RIN2 syndrome; MACS syndrome to Macrocephaly, alopecia, cutis laxa, and scoliosis, OMIM:613075
Ehlers Danlos syndrome with a likely monogenic cause v1.43 RIN2 Duncan Baker reviewed gene: RIN2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.42 RIN2 Eleanor Williams reviewed gene: RIN2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.41 RIN2 Eleanor Williams Source NHS GMS was added to RIN2.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Ehlers Danlos syndrome with a likely monogenic cause RIN2 Angela Brady reviewed RIN2
Ehlers Danlos syndrome with a likely monogenic cause RIN2 Neeti Ghali reviewed RIN2
Ehlers Danlos syndrome with a likely monogenic cause RIN2 Louise Daugherty classified RIN2 as green
Ehlers Danlos syndrome with a likely monogenic cause RIN2 Louise Daugherty edited their review of RIN2
Ehlers Danlos syndrome with a likely monogenic cause RIN2 Louise Daugherty commented on RIN2