Disease #06488 (NEDMABA (Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies), OMIM:618622)
Official abbreviation |
NEDMABA |
Name |
Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies |
OMIM ID |
618622 |
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 |
SMPD4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|