SUPERFAMILY 1.75 HMM library and genome assignments server

SUPERFAMILY 2 can be accessed from supfam.org. Please contact us if you experience any problems.

Disease Ontology (DO): multiple endocrine neoplasia type 1

(show info)

Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   genetic disease [DOID:630] <11>(19|28) (22|16|7)
+ + + 3:   monogenic disease [DOID:0050177] <7>(17|25) (19|14|6)
+ + 2:   autosomal genetic disease [DOID:0050739] <8>(17|24) (19|14|6)
+ 1:   autosomal dominant disease [DOID:0050736] <79>(7|13) (9|8|3)
0:   multiple endocrine neoplasia type 1 [DOID:10017](0|0) (0|0|0)