Genomics England
GMS Panels
Panels
Genes and Entities
HNMT
histamine N-methyltransferase
OMIM:
605238
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Panel
Mode of inheritance
Details
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Intellectual disability
Component of the following Super Panels:
- Hypotonic infant
- Leukodystrophy, childhood onset
- Paediatric disorders
Signed-off version 11.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mental retardation, autosomal recessive 51, OMIM:616739