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MIM:616362 - HOUGE-JANSSENS SYNDROME 2; HJS2
Xenbase Genes: ppp2r1a
Human Disease Resource: MIM
MONDO:0014605 - Houge-Janssens syndrome 2 |
DOID:0070066 - autosomal dominant intellectual developmental disorder 36 |
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MONDO:0014605 - Houge-Janssens syndrome 2 |
DOID:0070066 - autosomal dominant intellectual developmental disorder 36 |