Disease #00185 (AMD3 (dysplasia, acromesomelic, type 3, Demirhan), OMIM:609441)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	AMD3
Name	dysplasia, acromesomelic, type 3, Demirhan
OMIM ID	609441
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BMPR1B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-09-02 22:20:13 +02:00 (CEST)
Date last edited	2021-12-16 18:31:40 +01:00 (CET)

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