(Q55784298)

English

Wolfram-like syndrome

medical condition

WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT
WFSL
Hearing Loss, Progressive, With Optic Atrophy And/Or Impaired Glucose Regulation
WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL

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Statements

instance of

head and neck disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013673

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

0 references

developmental anomaly of metabolic origin

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013673

rare genetic diabetes mellitus

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013673

syndromic hereditary optic neuropathy

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013673

autoimmune disease of the nervous system

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013673

rare genetic immune disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0013673

syndromic genetic deafness

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

4 references

13 August 2019

WFS1 mutations in Spanish patients with diabetes mellitus and deafness

9 December 2020

https://search.clinicalgenome.org/kb/gene-validity/17637c9d-03fb-496a-a00c-ae2431f441e8--2018-04-17T04:00:00

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_17637c9d-03fb-496a-a00c-ae2431f441e8-2018-04-17T040000.000Z

exact match

http://www.orpha.net/ORDO/Orphanet_411590

0 references

Identifiers

PatientsLikeMe condition ID

wolfram-like-syndrome

0 references

ICD-10-CM

E13.8

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

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

28 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Wolfram-like syndrome

0 references

Sitelinks

Wikipedia(1 entry)

enwiki Wolfram-like syndrome

(Q55784298)

Wolfram-like syndrome

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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