Disease #00271 (SCKL2 (Seckel syndrome, type 2 (SCKL-2)), OMIM:606744)

Official abbreviation SCKL2
Name Seckel syndrome, type 2 (SCKL-2)
OMIM ID 606744
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene RBBP8
Associated tissues -
Disease features -
Remarks -
Date created 2013-11-22 15:16:48 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00004046 - PubMed: Shaheen 2014, Journal: Shaheen 2014 - F yes Saudi Arabia Arab - - - - SCKL2 microphthalmia, micrognathia, microglossia, and small teeth. Bilateral basal ganglia calcification and cerebellar calcification on brain MRI RBBP8 RBBP8 1 1 Fowzan Alkuraya
00080865 - PubMed: Trujillano 2017 no information from parents - - - - - - - - SCKL2 Seckel syndrome type 2 (OMIM:606744) RBBP8 RBBP8 1 1 Daniel Trujillano
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