syndromic X-linked intellectual disability Najm type
Go to external page http://purl.obolibrary.org/obo/MONDO_0010417
Najm type X-linked intellectual deficit is a rare cerebellar dysgenesis syndrome characterized by variable clinical manifestations ranging from mild intellectual deficit with or without congenital nystagmus, to severe cognitive impairment associated with cerebellar and pontine hypoplasia/atrophy and abnormalities of cortical development. [ Orphanet:163937 ]
Synonyms: intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia, X-linked dominant mental retardation and microcephaly with pontine and cerebellar hypoplasia intellectual disability and microcephaly with pontine and cerebellar hypoplasia syndromic X-linked intellectual disability Najm type MICPCH X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome
Term information
- DOID:0060807 (MONDO:equivalentTo)
- MESH:C567466 (MONDO:equivalentTo)
- GARD:12669 (MONDO:GARD)
- Orphanet:163937 (OMIM:300749)
- MEDGEN:437070 (MONDO:equivalentTo)
- UMLS:C2677903 (MONDO:equivalentTo)
- OMIM:300749 (Orphanet:163937/e)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
http://identifiers.org/medgen/437070
http://linkedlifedata.com/resource/umls/id/C2677903
http://www.orpha.net/ORDO/Orphanet_163937
http://identifiers.org/mesh/C567466
http://purl.obolibrary.org/obo/DOID_0060807
https://omim.org/entry/300749
intellectual disability, X-linked, syndromic, Najm type
mental retardation and microcephaly with PONTINE and cerebellar hypoplasia
X-linked intellectual disability - microcephaly - pontocerebellar hypoplasia
Micpch syndrome
intellectual disability and microcephaly with PONTINE and cerebellar hypoplasia
mental retardation, X-linked, syndromic, Najm type
X-linked intellectual disability, Najm type
microcephaly with pontine and cerebellar hypoplasia
https://github.com/monarch-initiative/mondo/issues/5588
https://github.com/monarch-initiative/mondo/issues/4521