Noun:

వ్యాధిలో అనేక లక్షణాలను చేర్చడం,

syndromic's Usage Examples:

In contrast, syndromic deafness involves hearing loss that occurs with.

retardation X linked syndromic 6 (MRXS6), and mental retardation X linked with gynecomastia and obesity is a congenital condition characterized by intellectual disability.

"A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss.

Mutations in gap junction genes have been found to lead to both syndromic and nonsyndromic deafness.

"X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family.

hearing impairment and a recessive form of sensorineural pre-lingual non-syndromic deafness.

Public health surveillance (also epidemiological surveillance, clinical surveillance or syndromic surveillance) is, according to the World Health Organization.

Non-syndromic hearing impairment protein 5 is a protein that in humans is encoded by the DFNA5 gene.

Studies have also shown increased levels of FA of ear length in individuals with cleft lip and/or non-syndromic cleft palate syndrome.

syndrome, and iso(18p), which is associated with mental retardation and syndromic facies.

Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms.

the bridge to liberation from disease) is an Indian COVID–19 "contact tracing, syndromic mapping and self-assessment" digital service, primarily a mobile.

absence of prominent lip pits, cannot be easily distinguished from non-syndromic forms of orofacial clefting.