(Q55784059)

English

Nestor-Guillermo progeria syndrome

human disease

Progeria Syndrome, Childhood-Onset, With Osteolysis
NESTOR-GUILLERMO PROGERIA SYNDROME
PSCOO
NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS
NGPS

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

class of disease

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

2 references

UniProt protein ID

13 August 2019

Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome

http://www.orpha.net/ORDO/Orphanet_280576

0 references

Identifiers

0 references

GARD rare disease ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(1 entry)

enwiki Nestor-Guillermo progeria syndrome

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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