Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Oliver-McFarlane syndrome
Summary
- Synonym
-
- OMCS
- eyelashes long mental retardation
- long eyelashes-intellectual disability syndrome
- trichomegaly-retina pigmentary degeneration-dwarfism syndrome
- Definition
- A syndrome characterized by trichomegaly, severe chorioretinal atrophy and multiple pituitary hormone deficiencies that has_material_basis_in homozygous or compound heterozygous mutation in PNPLA6 on 19p13.2.
- Super Class
- autosomal recessive disease syndrome
External Links
- Disease Ontology
- DOID:0111271
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- OMIM
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000546 | Retinal degeneration |
| HP:0000164 | Abnormality of the dentition |
| HP:0001249 | Intellectual disability |
| HP:0000054 | Micropenis |
| HP:0000821 | Hypothyroidism |
| HP:0001251 | Ataxia |
| HP:0000527 | Long eyelashes |
| HP:0000028 | Cryptorchidism |
| HP:0000580 | Pigmentary retinopathy |
| HP:0001250 | Seizure |
