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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/613630
http://purl.bioontology.org/ontology/OMIM/613630
|
|---|---|
| Preferred Name | FETAL ENCASEMENT SYNDROME |
| Synonyms |
COCOON SYNDROME
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | COCOON SYNDROME
|
|---|---|
| prefLabel | FETAL ENCASEMENT SYNDROME
|
| Gene Symbol |
BPS2
IKKA
CHUK
IKBKA
NFKBIKA
IKK1
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|
| Scope Statement | Based on report of 1 family (last curated June 2021) [MISCELLANEOUS]
Caused by mutation in the component of nuclear factor kappa-B kinase complex gene (CHUK, 600664.0001) [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 10q24
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 613630
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C3150891
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |