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Moynahan syndrome
human disease
Moynahan Alopecia Syndrome
Alopecia-epilepsy-intellectual disability syndrome, Moynahan type
ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN
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Statements
instance of
class of disease
0 references
subclass of
genetic syndromic intellectual disability
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
hyperpigmentation of the skin
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
epilepsy syndrome
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
exact match
http://www.orpha.net/ORDO/Orphanet_2574
0 references
Identifiers
MeSH descriptor ID
C537052
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
GARD rare disease ID
606
1 reference
stated in
Genetic and Rare Diseases Information Center
retrieved
1 April 2019
ICD-10-CM
G40.4
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
Mondo ID
MONDO_0008755
0 references
OMIM ID
203600
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
Orphanet ID
2574
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
UMLS CUI
C0265328
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008755
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Wikipedia
(1 entry)
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enwiki
Moynahan syndrome
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