Meckel syndrome 2
Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM216 on chromosome 11q12.2
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Meckel syndrome 2
Summary
Meckel syndrome 2 is a rare disease[1].
Key Facts
- Meckel syndrome 2's instance of is recorded as rare disease[2].
- Meckel syndrome 2's instance of is recorded as class of disease[3].
- Meckel syndrome 2's subclass of is recorded as Meckel syndrome[4].
- Meckel syndrome 2's MeSH descriptor ID is recorded as C536131[5].
- Meckel syndrome 2's OMIM ID is recorded as 603194[6].
- Meckel syndrome 2's Disease Ontology ID is recorded as DOID:0070116[7].
- Meckel syndrome 2's genetic association is recorded as TMEM216[8].
- Meckel syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070116[9].
- Meckel syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0070116[10].
- Meckel syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_564[11].
- Meckel syndrome 2's UMLS CUI is recorded as C1864148[12].
- Meckel syndrome 2's ICD-10-CM is recorded as Q61.9[13].
- Meckel syndrome 2's GARD rare disease ID is recorded as 8743[14].
- Meckel syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Meckel syndrome 2's Mondo ID is recorded as MONDO_0011296[16].
- Meckel syndrome 2's UniProt disease ID is recorded as DI-02862[17].