Disease #00034 (ACH (ACHONDROPLASIA), OMIM:100800)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

Official abbreviation	ACH
Name	ACHONDROPLASIA
OMIM ID	100800
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 0 genes	-
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-11 10:32:39 +00:00 (UTC)
Date last edited	2025-10-09 12:48:29 +00:00 (UTC)