| Human Disease |
Achalasia-Addisonianism-Alacrima Syndrome; AAAS OMIM ID: 231550 |
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| Synonyms | Addisonian-Achalasia Syndrome; Alacrima-Achalasia-Addisonianism; Alacrima-Achalasia-Adrenal Insufficiency Neurologic Disorder; Allgrove Syndrome; Glucocorticoid Deficiency and Achalasia; Hypoadrenalism with Achalasia; Triple-A Syndrome | |||||||||||||||||||||
| View all models | View ALL (1) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Aaastm1Ahue/Aaastm1Ahue |
involves: 129P2/OlaHsd * C57BL/6 | J:106908 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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