Genomics England
GMS Panels
Panels
Genes and Entities

SMPD4

sphingomyelin phosphodiesterase 4
OMIM: 610457
PanelMode of inheritanceDetails
5 panels
Green
in Arthrogryposis
R-numbers: R83
Signed-off version 8.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
cerebellar hypoplasia, hypomyelination, microcephaly, arthrogryposis
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Developmental Disorder with Microcephaly and Congenital Arthrogryposis
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.80
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies, OMIM:618622, Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies, MONDO:0032838
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.134
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
cerebellar hypoplasia, hypomyelination, microcephaly, arthrogryposis
Green
in Monogenic diabetes
R-numbers: R141
Signed-off version 2.60
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies, OMIM:618622, type 1 diabetes mellitus, MONDO:0005147