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1 OMIM reference -
1 associated gene
13 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Spondyloperipheral dysplasia - short ulna
Hyaluronidase deficiency

COL2A1 HYAL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
COL2A1
(0.63)
HYAL1



Citations in the biomedical literature:


Spondyloperipheral dysplasia - short ulna
COL2A1
Hyaluronidase deficiency
HYAL1



Spondyloperipheral dysplasia - short ulna
Hyaluronidase deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Mucopolysaccharidosis type 9

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare bone disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C535799
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Short stature / dwarfism / nanism


Spondyloperipheral dysplasia - short ulna
Hyaluronidase deficiency

Very frequent
- Abnormal vertebral size / shape
- Autosomal dominant inheritance
- Cone epiphyses / epiphysis
- Metacarpal anomalies / Archibald's sign
- Metaphyseal anomaly
- Short hand / brachydactyly

Frequent
- Epiphyseal vertebral anomaly
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality
- Restricted joint mobility / joint stiffness / ankylosis
- Short limbs / micromelia / brachymelia
- Ulnar / cubital anomaly / absence / agenesis / hypoplasia / abnormal ulnar / cubital ray

Occasional
- Pectus carinatum


Very frequent
- Autosomal recessive inheritance
- Subcutaneous nodules / lipomas / tumefaction / swelling