Disease #00105

Official abbreviation ACG-1B
Name achondrogenesis, type IB (ACG-1B)
OMIM ID 600972
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SLC26A2
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00080868 - Trujillano et al., submitted unaffected parents - - - - - 0 - - ACG-1B SLC26A2 SLC26A2 1 1 Daniel Trujillano
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