FAM160B1

family with sequence similarity 160 member B1
OMIM: 617312, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red FAM160B1 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	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Central hypotonia Global developmental delay Intellectual disability Abnormality of the face Tags new-gene-name

Panel

Reviews

Mode of inheritance

Details

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

BIALLELIC, autosomal or pseudoautosomal