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

HYAL1 COL2A1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hyaluronidase deficiency
HYAL1
Spondyloperipheral dysplasia - short ulna
COL2A1



Hyaluronidase deficiency
Spondyloperipheral dysplasia - short ulna

Synonym(s):
- Mucopolysaccharidosis type 9

Synonym(s):
(no synonyms)

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

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

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
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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


COMMON
SIGNS
- Short stature / dwarfism / nanism


Hyaluronidase deficiency
Spondyloperipheral dysplasia - short ulna

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



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