LADD syndrome
autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes
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LADD syndrome
Summary
LADD syndrome is a head and neck disease[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- LADD syndrome's instance of is recorded as head and neck disease[3].
- LADD syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- LADD syndrome's instance of is recorded as rare disease[5].
- LADD syndrome's instance of is recorded as class of disease[6].
- LADD syndrome's subclass of is recorded as autosomal dominant disease[7].
- LADD syndrome's subclass of is recorded as genetic otorhinolaryngological malformation[8].
- LADD syndrome's subclass of is recorded as syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[9].
- LADD syndrome's subclass of is recorded as EEC syndrome and related syndrome[10].
- LADD syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability[11].
- LADD syndrome's subclass of is recorded as malformation syndrome with odontal and/or periodontal component[12].
- LADD syndrome's subclass of is recorded as nose and cavum anomaly[13].
- LADD syndrome's subclass of is recorded as syndrome[14].
- LADD syndrome's Commons category is recorded as LADD syndrome[15].
- LADD syndrome's MeSH descriptor ID is recorded as C538132[16].
- LADD syndrome's OMIM ID is recorded as 149730[17].
- LADD syndrome's ICD-10 ID is recorded as Q87.8[18].
- LADD syndrome's KEGG ID is recorded as H00642[19].
- LADD syndrome's Disease Ontology ID is recorded as DOID:0050331[20].
- LADD syndrome's Orphanet ID is recorded as 2363[21].
- LADD syndrome's ICD-9-CM is recorded as 759.89[22].
- LADD syndrome's health specialty is recorded as medical genetics[23].
- LADD syndrome's genetic association is recorded as FGF10[24].
- LADD syndrome's genetic association is recorded as FGFR2[25].
- LADD syndrome's genetic association is recorded as FGFR3[26].
- LADD syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050331[27].
Why It Matters
LADD syndrome is known by 10 alternative names across languages and contexts.[2]