Disease #07084 (MSUD2 (maple syrup urine disease, type II), OMIM:620699)

Official abbreviation MSUD2
Name maple syrup urine disease, type II
OMIM ID 620699
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 DBT
Associated tissues -
Disease features -
Remarks -
Date created 2024-05-25 09:42:47 +02:00 (CEST)
Date last edited N/A


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00451439 3bINP-027 PubMed: Vela-Amieva 2024 Familial case (sister affected: died at 05m) F no Mexico Mexican - - - - MSUD2 Hypoglycemia, short stature, hip dysplasia DBT DBT 1 1 Miriam Erandi Reyna-Fabián
00451636 3bINP-076 PubMed: Vela-Amieva 2024 - F no Mexico Mexican - - - - MSUD2 Severe intellectual disability, Seizures, Opisthotonus DBT DBT 1 1 Miriam Erandi Reyna-Fabián
00451645 3bINP-081 PubMed: Vela-Amieva 2024 - M no Mexico Mexican - - - - MSUD2 Global developmental delay, Spasticity DBT DBT 2 1 Miriam Erandi Reyna-Fabián
00451652 3bINP-092 PubMed: Vela-Amieva 2024 Familial case (sister affected: died at 01m) F no Mexico Mexican - - - - MSUD2 Severe intellectual disability, Seizures, Spasticity, Dermatosis DBT DBT 1 1 Miriam Erandi Reyna-Fabián
00451653 3bINP-094 PubMed: Vela-Amieva 2024 Family case (affected maternal aunt and uncle) M yes Mexico Mexican - - - - MSUD2 Severe intellectual disability, Central hypothyroidism, Bilateral cryptorchidism DBT DBT 1 1 Miriam Erandi Reyna-Fabián
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