Disease #03608 (SCZD17 (schizophrenia, type 17 (SCZD17)), OMIM:614332)

Official abbreviation SCZD17
Name schizophrenia, type 17 (SCZD17)
OMIM ID 614332
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 5
Associated with 1 gene NRXN1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-07-21 14:11:39 +02:00 (CEST)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00377281 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377283 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377284 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377285 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377286 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377287 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377288 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
00377289 - - - - - - - - - - - SCZD17 - NRXN1 - 1 1 Emanuele Coci
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