Disease #03926 (MCAHS3;GPIBD7 (multiple congenital anomalies, hypotonia, seizures syndrome, type 3 (MCAHS-3, glycosylphosphatidylinositol deficiency, type 7 (GPIBD-7))), OMIM:615398)
Official abbreviation |
MCAHS3;GPIBD7 |
Name |
multiple congenital anomalies, hypotonia, seizures syndrome, type 3 (MCAHS-3, glycosylphosphatidylinositol deficiency, type 7 (GPIBD-7)) |
OMIM ID |
615398 |
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 |
PIGT |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|