Disease #00930 (Currarino (Currarino syndrome), OMIM:176450)

Official abbreviation Currarino
Name Currarino syndrome
OMIM ID 176450
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene MNX1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-15 11:07:36 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00248471 - - - - - - - - - - - Currarino - MNX1 MNX1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00445401 - - - - - - - - - - - Currarino - MNX1 MNX1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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