Disease #00780 (IPOX (intestinal pseudoobstruction, neuronal), OMIM:300048)
Official abbreviation |
IPOX |
Name |
intestinal pseudoobstruction, neuronal |
OMIM ID |
300048 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
FLNA |
Associated tissues |
- |
Disease features |
- |
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
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