Activity

Filter

Cancel
Date Panel Item Activity
5 actions
Rare multisystem ciliopathy disorders v1.134 B9D2 Arina Puzriakova Publications for gene: B9D2 were set to 21763481 - two affected fetuses form the same family displayed overlapping phenotypes including cystic kidneys, ductal plate malformation, polydactyly, and occipital encephalocele. Homozygous variant identified in this gene, which was not present in the unaffected son. Homozygous variants were not identified in other known Meckel syndrome genes; 26092869 - two further cases with Joubert syndrome reported from two different families
Rare multisystem ciliopathy disorders v1.133 B9D2 Arina Puzriakova commented on gene: B9D2
Rare multisystem ciliopathy disorders v1.133 B9D2 Arina Puzriakova Phenotypes for gene: B9D2 were changed from Meckel syndrome 10, 614175; ciliopathies; Meckel syndrome; Joubert syndrome to Joubert syndrome 34, OMIM:614175; Meckel syndrome 10, OMIM:614175; Meckel syndrome, type 10, MONDO:0013609
Rare multisystem ciliopathy disorders B9D2 Alice Gardham marked B9D2 as ready
Rare multisystem ciliopathy disorders B9D2 Alice Gardham commented on B9D2