Disease #05182 (IHPRF2 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 2 (IHPRF-2)), OMIM:616801)

Official abbreviation IHPRF2
Name hypotonia, infantile, with psychomotor retardation and characteristic facies, type 2 (IHPRF-2)
OMIM ID 616801
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene UNC80
Associated tissues -
Disease features -
Remarks -
Date created 2016-09-13 16:07:19 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00081054 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - IHPRF2 Hypotonia, infantile, with psychomotor retardation and characteristic facies 2 (OMIM:616801) UNC80 UNC80 1 1 Daniel Trujillano
00380804 ? PubMed: Nair 2018 - ? - Lebanon - - - - - IHPRF2 DD; ID; hypotonia, dysmorphic facial features; failure to thrive (Neurological) - UNC80 1 1 LOVD
00464364 - - - - no Italy - - - - - IHPRF2 Growth abnormality (HP:0001507); Dysphagia (HP:0002015); Delayed speech and language development (HP:0000750); Hypotonia (HP:0001252); Global developmental delay (HP:0001263); Seizure (HP:0001250) UNC80 UNC80 2 2 Mario Benvenuto
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