Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation

Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (disorder)

active

Code	`1304277005`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20240401

Synonyms

Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation
H1-4-related neurodevelopmental disorder
Rahman syndrome

Parents (2)

1362108000Genetic intellectual disability disorder
48637007Multiple malformation syndrome with early overgrowth disorder

Children (0)

None (leaf concept).