Disease #00191 (AMD2A (dysplasia, acromesomelic, type 2A, Grebe), OMIM:200700)

Official abbreviation AMD2A
Name dysplasia, acromesomelic, type 2A, Grebe
OMIM ID 200700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene GDF5
Associated tissues -
Disease features -
Remarks -
Date created 2013-09-08 14:51:28 +02:00 (CEST)
Date last edited 2021-12-16 17:35:12 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00002458 - PubMed: Graul-Neumann 2013 - F yes Lebanon lebanese - - - - AMD2A - BMPR1B BMPR1B 2 1 Sandra Doelken
00002459 - PubMed: Graul-Neumann 2013 family, 2 affecteds (IIa, IIb) M yes Pakistan pakistani - - - - AMD2A - BMPR1B BMPR1B 2 1 Sandra Doelken
00002460 - PubMed: Graul-Neumann 2013 family, 2 affecteds (IIa, IIb) M yes Pakistan pakistani - - - - AMD2A - BMPR1B BMPR1B 2 1 Sandra Doelken
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