Disease #00612 (CSA (Cockayne syndrome, type A (CSA)), OMIM:216400)

Official abbreviation CSA
Name Cockayne syndrome, type A (CSA)
OMIM ID 216400
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 3
Associated with 1 gene ERCC8
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

6 entries on 1 page. Showing entries 1 - 6.
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00057256 - PubMed: Rump 2016 - M yes - - - - - - CSA Microcephaly HP:0000252 - ERCC8 1 1 Birgit Sikkema-Raddatz
00373719 iw110 - - M no China Chinese - - - - CSA HP:0001276; HP:0001249; HP:0006817; HP:0000238; HP:0100702; HP:0001263; HP:0000750; HP:0001181; HP:0002194; HP:0010862; HP:0001883 ERCC8 ERCC8 2 1 Wenjuan Qiu
00416849 16 PubMed: Rump 2016 - M - - - - - - - CSA brain magnetic resonance imaging: leucodystrophy, cerebral and cerebellar atrophy; additional clinical featuresshort stature, truncal hypotonia, spasticity, contractures, scoliosis, deafness, pigmentary retinopathy, mildly enlarged liver and elevated aminotransferase, feeding problems, cryptorchid testis, severe developmental delay, progressive disease course (consanguineous parents) ERCC8 ERCC8 1 1 LOVD
00465605 - - - - - - - - - - - CSA - ERCC8 ERCC8 1 1 Min Peng
00465606 - - - - - - - - - - - CSA - ERCC8 ERCC8 1 1 Min Peng
00465607 - - - - - - - - - - - CSA - ERCC8 ERCC8 2 1 Min Peng
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