Disease #00175 (PRLMNS (PERLMAN SYNDROME), OMIM:267000)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	PRLMNS
Name	PERLMAN SYNDROME
OMIM ID	267000
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DIS3L2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-29 13:06:20 +00:00 (UTC)
Date last edited	N/A