Disease #04545 (MKS12 (Meckel syndrome?, type 12 (MKS-12)), OMIM:616258)

Official abbreviation MKS12
Name Meckel syndrome?, type 12 (MKS-12)
OMIM ID 616258
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 KIF14
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

5 entries on 1 page. Showing entries 1 - 5.
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00132082 - - - F yes - - - - - - MKS12 - - KIF14 1 2 Periklis Makrythanasis
00132083 - - - - - - - - - - - MKS12 - - KIF14 1 2 Periklis Makrythanasis
00132084 - - - - yes - - - - - - MKS12 - - KIF14 1 1 Periklis Makrythanasis
00132085 - - - - yes - - - - - - MKS12 - - KIF14 1 1 Periklis Makrythanasis
00181143 - - - F ? - - - - - - MKS12 Agenesis of corpus callosum (HP:0001274), Cerebral hypoplasia (HP:0006872), Arhinencephaly, Renal hypoplasia (HP:0000089), Cystic renal dysplasia (HP:0000800), Vaginal atresia (HP:0000148), Hypoplasia of the uterus (HP:0000013) KIF14 KIF14 2 1 Isabel Filges
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