Disease #00191

Official abbreviation AMDG
Name chondrodysplasia, acromesomelic, type Grebe (AMDG)
OMIM ID 200700
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 2 genes BMPR1B, GDF5
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00002458 - PubMed: Graul-Neumann 2013 - F yes Lebanon lebanese - 0 - - AMDG - BMPR1B BMPR1B 2 1 Sandra Doelken
00002459 - PubMed: Graul-Neumann 2013 family, 2 affecteds (IIa, IIb) M yes Pakistan pakistani - 0 - - AMDG - BMPR1B BMPR1B 2 1 Sandra Doelken
00002460 - PubMed: Graul-Neumann 2013 family, 2 affecteds (IIa, IIb) M yes Pakistan pakistani - 0 - - AMDG - BMPR1B BMPR1B 2 1 Sandra Doelken
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