(Q3321253)

English

chromosome 9p deletion syndrome

Human disease

9p syndrome
Alfi syndrome
monosomy 9p syndrome
CHROMOSOME 9p DELETION SYNDROME
Monosomy 9p
9p- syndrome
Monosomy type 9p
9p deletion syndrome

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Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

chromosomal deletion syndrome

1 reference

30 November 2020

partial deletion of the short arm of chromosome 9

0 references

health specialty

medical genetics

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

ICD-9-CM

758.39

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://purl.obolibrary.org/obo/DOID_0060732

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0060732

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_261112

0 references

Identifiers

MeSH descriptor ID

C538024

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

30 November 2020

2 references

28 August 2019

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Microsoft Academic ID

0 references

0 references

1 reference

28 August 2019

1 reference

28 August 2019

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

(Q3321253)

chromosome 9p deletion syndrome

Statements

Identifiers

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Wikipedia(4 entries)

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