FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Rett syndrome ID (Ontology) DOID:1206 (Human Disease)
Definition A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability.
Also Known As "cerebroatrophic hyperammonemia" ; "Rett's disorder"
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       5
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 Rett syndrome       6      8      1
 ameliorates | Rett syndrome       2       --       --
 for disease ribbon | Rett syndrome       --       6       --
 model of | Rett syndrome       4      6       --
Spanning Tree (Parents/Children)
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  developmental disorder of mental health
   |__pervasive developmental disorder
       |__Rett syndrome  15 rec.
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Is a pervasive developmental disorder
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Synonyms
  • "cerebroatrophic hyperammonemia" EXACT
    "Rett's disorder" EXACT
Secondary IDs
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GARD:5696
ICD10CM:F84.2
MESH:D015518
MIM:312750
MIM:613454
NCI:C75488
SNOMEDCT_US_2023_03_01:192583003
UMLS_CUI:C0035372