Disease #02053 (Reticular dysgenesis, OMIM:267500)

Official abbreviation -
Name Reticular dysgenesis
OMIM ID 267500
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 AK2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +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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00462237 Toraman - - F yes Turkey Turkish - - yes - Reticular dysgenesis Raine syndrome FAM20C FAM20C 1 1 Bayram Toraman
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