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Hoyeraal-Hreidarsson syndrome

Disease Summary
Associated Targets (7)
Tbio

6

Tchem

1


Explore Associated Targets
Mondo Description Hoyeraal-Hreidarsson syndrome (HHS) is a very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.
Uniprot Description A clinically severe variant of dyskeratosis congenita that is characterized by multisystem involvement, early onset in utero, and often results in death in childhood. Affected individuals show intrauterine growth retardation, microcephaly, cerebellar hypoplasia, delayed development, and bone marrow failure resulting in immunodeficiency.
Mondo Term and Equivalent IDs
MONDO:0018045:  Hoyeraal-Hreidarsson syndrome
GARD:0000346: 
MESH:C536068: 
Orphanet:3322: 
SCTID:707276009: 
UMLS:C1846142: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found