Disease #04095 (XIGIS;MRD25 (Xia-Xibbs syndrome (XIGIS, MRD25)), OMIM:615829)

Official abbreviation XIGIS;MRD25
Name Xia-Xibbs syndrome (XIGIS, MRD25)
OMIM ID 615829
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 3
Associated with 1 gene AHDC1
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

5 entries on 1 page. Showing entries 1 - 5.
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00111391 S_078 PubMed: Popp 2017, Journal: Popp 2017 - M no - - - - - - XIGIS;MRD25 Severe ID, behavioral anomalies, scoliosis, hernia, strabismus, short stature, microcephaly AHDC1 AHDC1 1 1 Bernt Popp
00226093 03216 - - F yes (Turkey) Kurdish 02y - - - XIGIS;MRD25 global developmental delay (HP:0001263), hypoplasia corpus callosum (HP:0002079), laryngomalacia (HP:0001601), lack of speech (HP:0001344) AHDC1 AHDC1 1 1 Evren Gumus
00234329 XG_F - - M ? Brazil - 14y - - - XIGIS;MRD25 convulsion, neurovelopmental disease, sleep apnea AHDC1 AHDC1 1 1 Augusto César Cardoso-dos-Santos
00408818 196079 - - F no Germany - - - - - XIGIS;MRD25 Bilateral tonic-clonic seizure, Generalized non-motor (absence) seizure, Global developmental delay, Neurodevelopmental delay AHDC1 AHDC1 1 1 Andreas Laner
00410019 - - - F no - - - - - - XIGIS;MRD25 - - AHDC1 1 1 Stefano Giuseppe Caraffi
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