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5 OMIM references -
5 associated genes
35 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3
1 OMIM reference -
1 associated gene
23 signs/symptoms
Ear-patella-short stature syndrome
Cabezas syndrome

CDC6 CUL4B
CDT1
ORC1
ORC4
ORC6


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CDT1
(0.65)
CUL4B



Citations in the biomedical literature:


Ear-patella-short stature syndrome
CDC6 CDT1 ORC1 ORC4 ORC6
Cabezas syndrome
CUL4B



Ear-patella-short stature syndrome
Cabezas syndrome

Synonym(s):
- Meier-Gorlin syndrome

Synonym(s):
- X-linked intellectual deficit, Cabezas type

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked recessive

External references:
5 OMIM references -
1 MeSH reference: C538012
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Hyperextensible joints / articular hyperlaxity
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Short stature / dwarfism / nanism


Ear-patella-short stature syndrome
Cabezas syndrome

Very frequent
- Autosomal recessive inheritance
- Delayed bone age
- Epiphyseal anomaly
- External auditory canal atresia / stenosis / agenesis
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Hypoplastic mandibula / partial absence of the mandibula
- Intrauterine growth retardation
- Microcephaly
- Micrognathia / retrognathia / micrognathism / retrognathism
- Microstomia / little mouth
- Microtia / cryptomicrotia / anotia / external auditory canal / pinnae aplasia / hypoplasia
- Narrowed / gracile diaphysis / diaphyses / long bones / dolichostenomelia
- Undescended / ectopic testes / cryptorchidia / unfixed testes

Frequent
- Camptodactyly of fingers
- Clavicle absent / abnormal
- Clinodactyly of fifth finger
- Clitoris / labia majora / labia minora / female external genitalia hypoplasia
- Craniostenosis / craniosynostosis / sutural synostosis
- Female pseudohermaphrodism / virilisation / clitoridomegaly
- High vaulted / narrow palate
- Hypoplastic maxillary bones / zygomatic bones / maxillary hypoplasia
- Low set ears / posteriorly rotated ears
- Patella absent / abnormal (excluding luxation)
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Rib structure anomalies

Occasional
- Breast tissue / mammary gland absence / aplasia
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Elbow dislocation
- Hearing loss / hypoacusia / deafness
- Hypospadias / epispadias / bent penis
- Micropenis / small penis / agenesis
- Thick lips


Very frequent
- Inguinal / inguinoscrotal / crural hernia
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia

Frequent
- Abnormal gait
- Blepharophimosis / short palpebral fissures
- Everted lower lip
- Generalized obesity
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Pes cavus
- Seizures / epilepsy / absences / spasms / status epilepticus
- Short foot / brachydactyly of toes
- Small / atrophic / hypoplastic testes / monorchism / microorchidism / anorchia
- Tremor
- Wasted (excluding lipodystrophy) / poorly muscled build / cachexy
- Wide space between 1st-2nd toes

Occasional
- Acanthosis nigricans
- Hyperhidrosis / increased sweating
- Immunodeficiency / increased susceptibility to infections / recurrent infections
- Kyphosis
- Late puberty / hypogonadism / hypogenitalism
- Syndactyly of toes