(Q111042753)

English

arthrogryposis multiplex congenita-4

human disease

AMC4
arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum
Zain syndrome

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No description defined

Statements

class of disease

0 references

autosomal recessive disease

1 reference

Disease Ontology

1 March 2022

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_0080980

1 reference

Disease Ontology

1 March 2022

Disease Ontology ID

http://identifiers.org/doid/DOID:0080980

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

1 March 2022

Disease Ontology ID

0 references

UniProt disease ID

0 references

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