FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Adams-Oliver syndrome ID (Ontology) DOID:0060227 (Human Disease)
Definition A syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs.
Also Known As "Adams Oliver syndrome"
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       3
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 Adams-Oliver syndrome       3      5
 ameliorates | Adams-Oliver syndrome       2       --
 for disease ribbon | Adams-Oliver syndrome       --       4
 model of | Adams-Oliver syndrome       1      4
Spanning Tree (Parents/Children)
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  disease
   |__syndrome
       |__Adams-Oliver syndrome  9 rec.
           |__Adams-Oliver syndrome 3 2 rec.
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Synonyms
  • "Adams Oliver syndrome" EXACT
Secondary IDs
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GARD:5739
MIM:100300
MIM:614219
MIM:615297
MIM:616028
MIM:PS100300
ORDO:974
SNOMEDCT_US_2023_03_01:34748004
UMLS_CUI:C0265268