midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
human disease
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midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
Summary
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis is a developmental defect during embryogenesis[1].
Key Facts
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis's instance of is recorded as developmental defect during embryogenesis[2].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis's instance of is recorded as class of disease[3].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis is a type of Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome[4].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis is a type of syndrome[5].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis is a type of X-linked recessive disease[6].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis's genetic association is recorded as AMMECR1[7].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111859[8].
- midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis's exact match is recorded as http://identifiers.org/doid/DOID:0111859[9].