Term Name: | Heimler syndrome 1 |
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Synonyms: | 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. |
Ontology: | Human Disease [DOID:0080623] ( DOID:0080623 ) |