(Q29982036)

English

Parietal foramina with cleidocranial dysplasia

human disease

PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA
PFMCCD
Parietal foramina with clavicular hypoplasia
Cleidocranial Dysplasia With Parietal Foramina
PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA; PFMCCD
Parietal foramina with cleidocranial dysostosis

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

parietal foramina

0 references

cleidocranial dysplasia

0 references

cleidocranial dysplasia and isolated cranial ossification defect

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

craniofacial disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

2 references

UniProt protein ID

13 August 2019

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2

Identifiers

MeSH descriptor ID

mapping relation type

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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(1 entry)

dewiki Foramina parietalia mit kleidokranialer Dysostose

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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