Cadds (CADDS)

Alias:
Zellweger-Like Contiguous Gene Deletion Syndrome
Contiguous Abcd1 Dxs1357e Deletion Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cadds, also known as zellweger-like contiguous gene deletion syndrome, is related to adrenoleukodystrophy and peroxisome biogenesis disorder 1a. An important gene associated with Cadds is ABCD1 (ATP Binding Cassette Subfamily D Member 1). Affiliated tissues include liver and brain, and related phenotypes are global developmental delay and cholestasis
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
<1/1000000
2
12
--

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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