(Q11897418)

English

hepatic fibrosis-renal cysts-intellectual disability syndrome

human disease

CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZ SYNDROME AND MECKEL SYNDROME
Thompson-Baraitser syndrome

In more languages

Statements

class of disease

0 references

familial cystic renal disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

rare parenchymal liver disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic parenchymatous liver disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic syndromic intellectual disability

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_2031

0 references

Identifiers

Google Knowledge Graph ID

0 references

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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Sitelinks

Wikipedia(1 entry)

fiwiki Thompson–Baraitserin oireyhtymä

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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