ORPHA:726667
Houge-Janssens syndrome type 4
Synonyms: PPP2R5C-related neurodevelopmental disorder · PPP2R5C-related Houge-Janssens syndrome · HJS4
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Autosomal dominant
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Houge-Janssens syndrome type 4 | PPP2R5C-related neurodevelopmental disorder · PPP2R5C-related Houge-Janssens syndrome · HJS4 |
| fr | Syndrome de Houge-Janssens type 4 | Trouble du neurodéveloppement associé à PPP2R5C · Syndrome de Houge-Janssens associé à PPP2R5C |
| de | Houge-Janssens-Syndrom Typ 4 | HJS4 · PPP2R5C-assoziiertes Houge-Janssens-Syndrom · PPP2R5C-assoziierte neurologische Entwicklungsstörung |
| es | Síndrome de Houge-Janssens tipo 4 | SHJ4 · Síndrome de Houge-Janssens asociado al gen PPP2R5C · Trastorno del neurodesarrollo asociado al gen PPP2R5C |
| it | Sindrome di Houge-Janssens tipo 4 | HJS4 · Sindrome di Houge-Janssens correlata a PPP2R5C · Malattia del neurosviluppo correlata a PPP2R5C |
| nl | Syndroom van Houge-Janssens type 4 | HJS4 · PPP2R5C-gerelateerd syndroom van Houge-Janssens · PPP2R5C-gerelateerde neurologische ontwikkelingsstoornis |
| pt | Houge-Janssens syndrome type 4 | |
| pl | Houge-Janssens syndrome type 4 | = en |
| cs | Houge-Janssens syndrome type 4 | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 621185 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:726644Houge-Janssens syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare neurological diseases
No children.
4
Genes
1 direct| Gene | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|
| PPP2R5C | Disease-causing germline mutation(s) in | Assessed | HGNC:9311 | ENSG00000078304 | 601645 | 14q32.31 | protein phosphatase 2 regulatory subunit B'gamma | 25972378[PMID]_39978342[PMID] |
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/726667
- This record as JSON: /data/d/726667.json