Meckel syndrome 3
Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1
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Meckel syndrome 3
Summary
Meckel syndrome 3 is a rare disease[1].
Key Facts
- Meckel syndrome 3's instance of is recorded as rare disease[2].
- Meckel syndrome 3's instance of is recorded as class of disease[3].
- Meckel syndrome 3's subclass of is recorded as Meckel syndrome[4].
- Meckel syndrome 3's MeSH descriptor ID is recorded as C536132[5].
- Meckel syndrome 3's OMIM ID is recorded as 607361[6].
- Meckel syndrome 3's Disease Ontology ID is recorded as DOID:0070117[7].
- Meckel syndrome 3's genetic association is recorded as TMEM67[8].
- Meckel syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070117[9].
- Meckel syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0070117[10].
- Meckel syndrome 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_564[11].
- Meckel syndrome 3's UMLS CUI is recorded as C1846357[12].
- Meckel syndrome 3's ICD-10-CM is recorded as Q61.9[13].
- Meckel syndrome 3's GARD rare disease ID is recorded as 8744[14].
- Meckel syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Meckel syndrome 3's Mondo ID is recorded as MONDO_0011821[16].
- Meckel syndrome 3's UniProt disease ID is recorded as DI-00701[17].