Disease #00121 (TPBS (brachydactyly, Temtamy, preaxial, syndrome (TPBS)), OMIM:605282)

Official abbreviation TPBS
Name brachydactyly, Temtamy, preaxial, syndrome (TPBS)
OMIM ID 605282
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CHSY1
Associated tissues -
Disease features -
Remarks -
Date created 2013-04-18 09:31:07 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
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00001197 - - - F yes Egypt Middle Eastern - - - - TPBS - CHSY1 CHSY1 1 1 Mohamed
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