Disease #00565 (PTHSL-2 (Pitt-Hopkins-like syndrome 2 (PTHSL-2)), OMIM:614325)

Official abbreviation PTHSL-2
Name Pitt-Hopkins-like syndrome 2 (PTHSL-2)
OMIM ID 614325
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NRXN1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A