DPH2

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber DPH2 in Intellectual disability Level 2: Developmental disorders Version 11.23 Latest signed off version: v11.0 (12 Aug 2026) Component of the following Super Panels: Hypotonic infant Leukodystrophy, childhood onset Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Developmental delay with short stature, dysmorphic facial features, and sparse hair 2, OMIM:620062 developmental delay with short stature, dysmorphic facial features, and sparse hair 2, MONDO:0100217 Tags Q2_26_promote_green

Panel

Reviews

Mode of inheritance

Details

Level 2: Developmental disorders
Version 11.23
Latest signed off version: v11.0 (12 Aug 2026)

Component of the following Super Panels:

Hypotonic infant

Leukodystrophy, childhood onset

Paediatric disorders

review

BIALLELIC, autosomal or pseudoautosomal

Developmental delay with short stature, dysmorphic facial features, and sparse hair 2, OMIM:620062
developmental delay with short stature, dysmorphic facial features, and sparse hair 2, MONDO:0100217