Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay (CLIFAHDD)

Alias:
Congenital Limbs-Face Contractures-Hypotonia-Developmental Delay Syndrome
Clifahdd Syndrome
Clifahdd
Contractures, Limbs and Face, Congenital, Hypotonia, and Developmental Delay
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay, also known as congenital limbs-face contractures-hypotonia-developmental delay syndrome, is related to congenital contractures and hypotonia. An important gene associated with Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay is NALCN (Sodium Leak Channel, Non-Selective), and among its related pathways/superpathways are Ion channel transport and Interleukin-6 family signaling. Affiliated tissues include brain and temporal lobe, and related phenotypes are neurodevelopmental delay and arthrogryposis multiplex congenita
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Antenatal
<1/1000000
12
93
11

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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IF
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