Disease #01016 (AOS2 (Adams-Oliver syndrome, type 2 (AOS-2)), OMIM:614219)

Official abbreviation AOS2
Name Adams-Oliver syndrome, type 2 (AOS-2)
OMIM ID 614219
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 4
Associated with 1 gene DOCK6
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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00296754 - - - M no (China) - - - - - AOS2 no microcephaly (-HP000252), no scalp defects, no developmental delay, no dilatation DOCK6 DOCK6 2 1 Yan Cai
00391870 059P - - M no Spain - - - - - AOS2, ID - - DOCK6 2 1 Alejandro Brea-Fernández
00417195 - - Non-consanguineous family with two affected children - no Mexico - - - - - AOS2 microcephaly (<3rd centile, HP:0000252), aplasia cutis congenita scalp (HP:0007385), global developmental delay (HP:0001263) - DOCK6 1 1 Martin Zenker
00446573 - - - F no Spain - - - - - AOS2 aplasia cutis congenita of the scalp (HP:0007385); hypertelorism (HP:0000316); vitreoretinal abnormalities, congenita (HP:0007773); cutis marmorata (HP:0000965); calcifications of cerebral ventricles - DOCK6 2 1 Maria Elena García Paya
00466389 342561 - - F no ? (unknown) - - - - - AOS2 Neurodevelopmental delay, Microcephaly, Abnormality of the distal phalanges of the toes, Abnormal distal phalanx morphology of finger, 2-3 toe syndactyly DOCK6 DOCK6 1 1 Andreas Laner
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