Disease #05542 (BSS (Baratela-Scott syndrome (BSS)), OMIM:300881)

Official abbreviation BSS
Name Baratela-Scott syndrome (BSS)
OMIM ID 300881
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 12
Phenotype entries for this disease 12
Associated with 1 gene XYLT1
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2018-12-25 16:52:39 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

12 entries on 1 page. Showing entries 1 - 12.
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00210039 30554721-Fam01Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 3 1 Johan den Dunnen
00210040 30554721-Fam02Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 4 1 Johan den Dunnen
00210041 30554721-Fam03Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 2 1 Johan den Dunnen
00210042 30554721-Fam04Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 3 1 Johan den Dunnen
00210043 30554721-Fam05Pat1 PubMed: LaCroix 2018 2-generation family, affected brothers, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 3 2 Johan den Dunnen
00210044 30554721-Fam05Pat4 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 4 1 Johan den Dunnen
00210045 30554721-Fam06Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents F - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 3 1 Johan den Dunnen
00210046 30554721-Fam07Pat1 PubMed: LaCroix 2018 2-generation family, affected brothers, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 2 2 Johan den Dunnen
00210047 30554721-Fam07Pat4 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 3 1 Johan den Dunnen
00210048 30554721-Fam08Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 2 1 Johan den Dunnen
00210049 30554721-Fam09Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 1 1 Johan den Dunnen
00210050 30554721-Fam10Pat1 PubMed: LaCroix 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BSS see paper; short stature, facial dysmorphisms, developmental delay, skeletal dysplasia, … XYLT1 XYLT1 1 1 Johan den Dunnen
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