(Q2092226)

English

Pickardt syndrome

Rare form of tertiary hypothyroidism

Pickardt-Fahlbusch syndrome
Pituitary stalk interruption syndrome
Ectopic neurohypophysis
PSIS
Hypoplastic Anterior Pituitary, Missing Stalk, and Ectopic Posterior Pituitary

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default values for all languages

No label defined

No description defined

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Statements

instance of

class of disease

0 references

subclass of

pituitary gland disease

0 references

non-acquired pituitary hormone deficiency

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0019828

Pituitary stalk interruption syndrome

0 references

0 references

0 references

1 reference

Open Targets Platform

retrieved

24 August 2023

reference URL

https://platform.opentargets.org/evidence/ENSG00000175325/EFO_0001380

based on heuristic

inferred from an Open Targets association score over 0.7

NCI Thesaurus ID

C121150

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_95496

0 references

Identifiers

DiseasesDB

6314

1 reference

imported from Wikimedia project

English Wikipedia

Experimental Factor Ontology ID

0001380

1 reference

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

GARD rare disease ID

13209

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

imported from Wikimedia project

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

0 references

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0019828

(Q2092226)

Pickardt syndrome

Statements

Identifiers

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Wikipedia(3 entries)

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