HIST1H4D

histone cluster 1 H4 family member d
OMIM: 602823, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red HIST1H4D in Intellectual disability Level 2: Developmental disorders Version 9.279 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, imprinted status unknown	Sources Expert Review Red Literature Phenotypes Global developmental delay Intellectual disability Microcephaly Growth abnormality Abnormality of the face Tags new-gene-name

Panel

Reviews

Mode of inheritance

Details

Level 2: Developmental disorders
Version 9.279
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, imprinted status unknown