brain abnormalities, neurodegeneration, and dysosteosclerosis
MONDO:0032772Mondo
Findings
No curated finding names brain abnormalities, neurodegeneration, and dysosteosclerosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Juvenile onset · Progressive · Childhood onset
HPO, annotations 2026-09-02
Features
38 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Cerebral calcificationHPOHP:0002514
- 4 of 4 reported patients
- Diaphyseal sclerosisHPOHP:0003034
- 4 of 4 reported patients
- Increased skull ossificationHPOHP:0004330
- 4 of 4 reported patients
- Metaphyseal wideningHPOHP:0003016
- 4 of 4 reported patients
- PlatyspondylyHPOHP:0000926
- 4 of 4 reported patients
- VentriculomegalyHPOHP:0002119
- 4 of 4 reported patients
- SpasticityHPOHP:0001257
- 3 of 4 reported patients
- Craniofacial osteosclerosisHPOHP:0005464
- 2 of 4 reported patients
- Enlarged cisterna magnaHPOHP:0002280
- 2 of 4 reported patients
- Focal-onset seizureHPOHP:0007359
- 2 of 4 reported patients
- HydrocephalusHPOHP:0000238
- 2 of 4 reported patients · Congenital onset
- Hyperintensity of cerebral white matter on MRIHPOHP:0030890
- 2 of 4 reported patients
Show the remaining 26
- Sclerotic vertebral bodyHPOHP:0100861
- 2 of 4 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 4 reported patients
- Bell-shaped thoraxHPOHP:0001591
- 1 of 4 reported patients
- Bulbous noseHPOHP:0000414
- 1 of 4 reported patients
- Chiari type I malformationHPOHP:0007099
- 1 of 4 reported patients
- Cognitive impairmentHPOHP:0100543
- 1 of 4 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CSF1RHGNC:2433
- Definitive · G2P · Autosomal recessive · 2023
- Definitive · ClinGen · Autosomal recessive · 2026
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
Where it sits
- A kind of