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Intellectual disability syndromic and non-syndromic v0.6075 RBBP5 Ain Roesley Phenotypes for gene: RBBP5 were changed from to neurodevelopmental disorder MONDO:0700092, RBBP5-related
Intellectual disability syndromic and non-syndromic v0.6074 RBBP5 Ain Roesley edited their review of gene: RBBP5: Changed phenotypes: neurodevelopmental disorder MONDO:0700092, RBBP5-related
Intellectual disability syndromic and non-syndromic v0.6067 RBBP5 Ain Roesley Marked gene: RBBP5 as ready
Intellectual disability syndromic and non-syndromic v0.6067 RBBP5 Ain Roesley Gene: rbbp5 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.6067 RBBP5 Ain Roesley Classified gene: RBBP5 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.6067 RBBP5 Ain Roesley Gene: rbbp5 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.6067 RBBP5 Ain Roesley Classified gene: RBBP5 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.6067 RBBP5 Ain Roesley Gene: rbbp5 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.6066 RBBP5 Ain Roesley gene: RBBP5 was added
gene: RBBP5 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: RBBP5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RBBP5 were set to 39036895
Review for gene: RBBP5 was set to GREEN
gene: RBBP5 was marked as current diagnostic
Added comment: 5x Indivs (4x de novo) = 3x PTCs + 2x missense

4/5 dev delay/ID
2/5 short stature (<=-3 SD) + 2/5 <= -2 SD
1/5 microcephaly (<= -3 SD) + 3/5 <= -2 SD
2/5 SNHL
2/5 seizures
3/5 hypotonia
Sources: Literature