All diseases

OMIM ID
610954
OMIM term:
PITT-HOPKINS SYNDROME; PTHS
Alternative terms:
ENCEPHALOPATHY, SEVERE EPILEPTIC, WITH AUTONOMIC DYSFUNCTION
MENTAL RETARDATION, SYNDROMAL, WITH INTERMITTENT HYPERVENTILATION
(∗) Location:
18q21.2  
(†) Associated OMIM genes:
TCF4  
(‡) Associated MGI genes:

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