Sheldon-Hall syndrome

Summary

Sheldon-Hall syndrome is a rare disease^[1].

Key Facts

• Sheldon-Hall syndrome's instance of is recorded as rare disease^[2].
• Sheldon-Hall syndrome's instance of is recorded as class of disease^[3].
• Sheldon-Hall syndrome's subclass of is recorded as distal arthrogryposis^[4].
• Sheldon-Hall syndrome's Commons category is recorded as Sheldon-Hall syndrome^[5].
• Sheldon-Hall syndrome's MeSH descriptor ID is recorded as C538400^[6].
• Sheldon-Hall syndrome's OMIM ID is recorded as 601680^[7].
• Sheldon-Hall syndrome's ICD-10 ID is recorded as Q68.8^[8].
• Sheldon-Hall syndrome's Disease Ontology ID is recorded as DOID:0111599^[9].
• Sheldon-Hall syndrome's Orphanet ID is recorded as 1147^[10].
• Sheldon-Hall syndrome's health specialty is recorded as medical genetics^[11].
• Sheldon-Hall syndrome's genetic association is recorded as TNNT3^[12].
• Sheldon-Hall syndrome's genetic association is recorded as TNNI2^[13].
• Sheldon-Hall syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111599^[14].
• Sheldon-Hall syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111599^[15].
• Sheldon-Hall syndrome's UMLS CUI is recorded as C1834523^[16].
• Sheldon-Hall syndrome's Medical Dictionary for Regulatory Activities ID is recorded as 10062344^[17].
• Sheldon-Hall syndrome's GARD rare disease ID is recorded as 9909^[18].
• Sheldon-Hall syndrome's ICD-11 ID is recorded as 1206883656^[19].