autosomal recessive nonsyndromic deafness 28

autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the TRIOBP gene on chromosome 22q13

Wikidata entity: Q28024612

P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2293 genetic association ... Q18036107 (TRIOBP) TRIOBP
P31 instance of ... Q55789477 (head and neck disease) head and neck disease
P31 instance of ... Q112193867 (class of disease) class of disease
P31 instance of ... Q929833 (rare disease) rare disease
P1748 NCI Thesaurus ID String C129023 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P279 subclass of ... Q18553310 (autosomal recessive nonsyndromic deafness) autosomal recessive nonsyndromic deafness
External Ids
P699Disease Ontology IDDOID:0110486
P4229ICD-10-CMH90.3
P486MeSH descriptor IDC565218
P5270Mondo IDMONDO_0012355
P492OMIM ID609823
P492OMIM ID609823
P2892UMLS CUIC1853276
P11430UniProt disease IDDI-00868

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