CMIP

c-Maf inducing protein
OMIM: 610112, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CMIP in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • HP:0012759
    • HP:0000717
    • HP:0007018
    • HP:0001250
    • HP:0011471