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

MVZ für Humangenetik Regensburg

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Official abbreviation	ACH
Name	ACHONDROPLASIA
OMIM ID	100800
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FGFR3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-11 10:32:39 +00:00 (UTC)
Date last edited	2016-07-11 10:34:21 +00:00 (UTC)