Genomics England

cell adhesion associated, oncogene regulated

Panel	Mode of inheritance	Details
Filter panels5 panels
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 3.79	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes HOLOPROSENCEPHALY 11 614226
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 3.122	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes HOLOPROSENCEPHALY 11
Green in Holoprosencephaly - NOT chromosomal Component of the following Super Panels: - Cerebral malformation R-numbers: R85 Signed-off version 4.4	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Holoprosencephaly 11, 614226, Holoprosencephaly
Green in Intellectual disability Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 5.343	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Holoprosencephaly 11, 614226, HOLOPROSENCEPHALY 11
Green in Structural eye disease R-numbers: R36 Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Holoprosencephaly 11, OMIM:614226, MONDO:0013642