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Serkal syndrome
genetic disorder
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
sex differentiation disease
0 references
genetic association
WNT4
1 reference
stated in
SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4
Identifiers
KEGG ID
H02317
0 references
GARD rare disease ID
10302
0 references
Mondo ID
MONDO_0012734
0 references
OMIM ID
611812
0 references
Orphanet ID
139466
0 references
UMLS CUI
C2678492
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
UniProt disease ID
DI-01613
0 references
Sitelinks
Wikipedia
(2 entries)
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enwiki
SERKAL syndrome
ruwiki
Синдром SERKAL
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Wikinews
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Wikiquote
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Wikisource
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Wikiversity
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Wikivoyage
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Wiktionary
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Multilingual sites
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