Disease #04379 (BBS7 (Bardet-Biedl syndrome, type 7 (BBS-7)), OMIM:615984)

Official abbreviation BBS7
Name Bardet-Biedl syndrome, type 7 (BBS-7)
OMIM ID 615984
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 BBS7
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
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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00276326 - - - M yes Turkey - 05y - - - BBS7 Obesity Polydactyly ID Renal abnormalities Genital abnormalities Behavioral problems Facial dysmorphism Cardiac abnormalities BBS7 BBS7 1 1 Evren Gümüş
00483906 383751 - - F ? ? (unknown) - - - - - BBS7 Autistic behavior, Intellectual disability, Motor delay, Delayed speech and language development, Obesity, Polydactyly, Postaxial polydactyly, Attention deficit hyperactivity disorder, Astigmatism, Hypermetropia BBS7 BBS7 2 1 Andreas Laner
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