Activity

Filter

Cancel
Date Panel Item Activity
6 actions
Fetal anomalies v0.4207 NME8 Zornitza Stark Marked gene: NME8 as ready
Fetal anomalies v0.4207 NME8 Zornitza Stark Gene: nme8 has been classified as Green List (High Evidence).
Fetal anomalies v0.4207 NME8 Zornitza Stark Publications for gene: NME8 were set to PubMed: 12032915, 12483741, 12928894
Fetal anomalies v0.4183 NME8 Chirag Patel Classified gene: NME8 as Green List (high evidence)
Fetal anomalies v0.4183 NME8 Chirag Patel Gene: nme8 has been classified as Green List (High Evidence).
Fetal anomalies v0.4182 NME8 Chirag Patel gene: NME8 was added
gene: NME8 was added to Fetal anomalies. Sources: Literature
Mode of inheritance for gene: NME8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NME8 were set to PubMed: 12032915, 12483741, 12928894
Phenotypes for gene: NME8 were set to CINCA syndrome, OMIM # 607115
Review for gene: NME8 was set to GREEN
Added comment: Chronic infantile neurologic cutaneous and articular (CINCA) syndrome also known as 'neonatal onset multisystem inflammatory disease,' or NOMID, is a rare congenital inflammatory disorder characterized by a triad of neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation. 14 families with heterozygous missense mutations in exon 3. Presenting perinatally so suitable for fetal anomalies panel.
Sources: Literature