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1 OMIM reference -
1 associated gene
21 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3
1 OMIM reference -
1 associated gene
16 signs/symptoms
Hypochondroplasia
Autosomal dominant hypophosphatemic rickets

FGFR3 FGF23


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FGFR3
(0.52)
FGF23



Citations in the biomedical literature:


Hypochondroplasia
FGFR3
Autosomal dominant hypophosphatemic rickets
FGF23



Hypochondroplasia
Autosomal dominant hypophosphatemic rickets

Synonym(s):
(no synonyms)

Synonym(s):
- ADHR
- Autosomal dominant hypophosphatemia

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease

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

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

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


COMMON
SIGNS
- Autosomal dominant inheritance
- Rachidian / spine canal stenosis
- Short stature / dwarfism / nanism


Hypochondroplasia
Autosomal dominant hypophosphatemic rickets

Very frequent
- Abnormal vertebral size / shape
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Short foot / brachydactyly of toes
- Short hand / brachydactyly
- Short limbs / micromelia / brachymelia

Frequent
- Elbow anomalies(excluding luxation)
- Femur anomaly / absence / agenesis / hypoplasia / bifurcation
- Genu varum
- Hyperextensible joints / articular hyperlaxity
- Metaphyseal anomaly
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality

Occasional
- Apnea / sleep apnea
- Bowed diaphysis / diaphyses / long bones
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Lordosis
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Osteoarthritis
- Scoliosis


Very frequent
- Asthenia / fatigue / weakness
- Bone pain
- Hypophosphatemia
- Muscle weakness / flaccidity
- Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets

Frequent
- Mutiple fractures / bone fragility
- Periarticular tissue anomaly / extraarticular calcifications

Occasional
- Anomalies of teeth and dentition
- Heart / cardiac failure
- Myocardium anomalies / myocarditis
- Obnubilation / coma / lethargia / desorientation
- Seizures / epilepsy / absences / spasms / status epilepticus
- Structural anomalies of the respiratory system and diaphragm