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Human Disease
Heimler syndrome 1
- Term ID
- DOID:0080623
- Synonyms
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- Deafness-enamel hypoplasia-nail defects syndrome
- peroxisomal biogenesis disorder 1C
- Definition
- A peroxisomal biogenesis disorder that is characterized by sensorineural hearing loss, generalised enamel hypoplasia of the permanent dentition with normal primary dentition, and nail defects and has_material_basis_in homozygous or compound heterozygous mutations in the PEX1 gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/26387595
- References
- Ontology
- Human Disease ( DOID:0080623 )
- is a type of
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Genes Involved
Zebrafish Models