Disease #00191 (AMDG (chondrodysplasia, acromesomelic, type Grebe (AMDG)), OMIM:200700)

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	Curator: Johan T. den Dunnen

Official abbreviation	AMDG
Name	chondrodysplasia, acromesomelic, type Grebe (AMDG)
OMIM ID	200700
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	BMPR1B, GDF5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-09-08 14:51:28 +02:00 (CEST)
Date last edited	N/A