Disease #05268 (SCKL1 (Seckel syndrome, type 1), OMIM:210600)

Official abbreviation SCKL1
Name Seckel syndrome, type 1
OMIM ID 210600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene ATR
Associated tissues -
Disease features -
Remarks -
Date created 2017-05-18 15:07:04 +02:00 (CEST)
Date last edited 2023-03-14 15:38:48 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00114688 - PubMed: Willems 2010 Microdontia, Pyelic ectasia F - Morocco - - - - - SCKL1 Mild intellectual disability PCNT PCNT 1 1 Emmelien Aten
00114692 - PubMed: Willems 2010 Horseshoe kidney. Clinodactyly of fifth finger. Rupture of CNS vessels leading to death (20 years) M - France - - - - - SCKL1 Mild intellectual disability PCNT PCNT 1 1 Emmelien Aten
00114696 - PubMed: Willems 2010 Cafe au lait spots, areas of depigmention Hepatic cytolysis. Subglottic stenosis Recurrent upper respiratory tract infections F - Morocco - - - - - SCKL1 - PCNT PCNT 1 1 Emmelien Aten
00114697 - PubMed: Willems 2010 Sparse scalp hair. Receding forehead. Prominent curved nose, Micrognatia. Low set ears. Clinodactyly. Highpitched voice. Stridor. Upper respiratory tract infections M - Lebanon - - - - - SCKL1 intellectual disability PCNT PCNT 1 1 Emmelien Aten
00114699 - PubMed: Willems 2010 Cafe au lait spots, area of depigmentation. Polycystic ovaries. Chromosomal breakage F - Pakistan - - - - - SCKL1 - PCNT PCNT 1 1 Emmelien Aten
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