IGF1

insulin like growth factor 1
OMIM: 147440
PanelMode of inheritanceDetails
5 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
INSULIN-LIKE GROWTH FACTOR I DEFICIENCY 608747
R-numbers: R21
Signed-off version 1.92
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
INSULIN-LIKE GROWTH FACTOR I DEFICIENCY
R-numbers: R147
Signed-off version 1.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Insulin-Like Growth Factor I Deficiency, Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747, IGF1
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747, INSULIN-LIKE GROWTH FACTOR I DEFICIENCY (IGF1 DEFICIENCY)
R-numbers: R88
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747, MPD, microcephalic primordial dwarfism