(Q26695317)

English

Hermansky-Pudlak syndrome 5

Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the HPS5 gene on chromosome 11p14

Hermansky-Pudlak syndrome type 5
HERMANSKY-PUDLAK SYNDROME 5
HPS5
HERMANSKY-PUDLAK SYNDROME 5; HPS5

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class of disease

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subclass of

Hermansky-Pudlak syndrome

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30 November 2020

1 reference

13 August 2019

on focus list of Wikimedia project

WikiProject Medicine

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exact match

http://purl.obolibrary.org/obo/DOID_0060543

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0060543

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Identifiers.org

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

Identifiers

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30 November 2020

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1 reference

28 August 2019

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

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