Lacrimoauriculodentodigital Syndrome 1 (LADD1)

Alias:
Ladd Syndrome
Levy-Hollister Syndrome
Lacrimoauriculodentodigital Syndrome
Ladd Syndrome 1
Lacrimo-Auriculo-Dento-Digital Syndrome 1
Lacrimoauriculoradiodental Syndrome
Lard Syndrome
Ladd1
Congenital Duodenal Obstruction Due to Malrotation of Intestine
Lacrimo-Auriculo-Dento-Digital Syndrome
Lacrimo-Auriculo-Dento-Digital Syndrome
Ladd1 Syndrome
Ladd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Lacrimoauriculodentodigital Syndrome 1, also known as ladd syndrome, is related to dacryocystocele and aplasia of lacrimal and salivary glands. An important gene associated with Lacrimoauriculodentodigital Syndrome 1 is FGFR2 (Fibroblast Growth Factor Receptor 2), and among its related pathways/superpathways are Infectious disease and Apoptotic Pathways in Synovial Fibroblasts. Affiliated tissues include eye and kidney, and related phenotypes are abnormality of the dentition and carious teeth
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Antenatal
<1/1000000
26
364
15

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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