Disease #06101 (PAMDDFS (Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures), OMIM:618737)

Official abbreviation	PAMDDFS
Name	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
OMIM ID	618737
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TUBGCP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.

Global Variome shared LOVD