All diseases

OMIM ID
300523
OMIM term:
ALLAN-HERNDON-DUDLEY SYNDROME; AHDS
Alternative terms:
ALLAN-HERNDON SYNDROME
MONOCARBOXYLATE TRANSPORTER 8 DEFICIENCY
TRIIODOTHYRONINE RESISTANCE
T3 RESISTANCE
MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA
MENTAL RETARDATION AND MUSCULAR ATROPHY
(∗) Location:
Xq13.2  
(†) Associated OMIM genes:
SLC16A2  
(‡) Associated MGI genes:
Slc16a2  

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