Phenotypes for disease #00594 (ACH (achondroplasia (ACH)), OMIM:100800)

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Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000299073 see paper; ..., short at birth; normal motor and mental milestones; height was 67.5 cm (-7.1 SD), short limbs, OFC 47 cm; acromesomelia, facial abnormalities, frontal bossing, prominent eyes, hypertelorism, flat nasal bridge, anteverted nostrils, folded low set ears, tented upper lip, wide mouth, gum hypertrophy suggestive of 'fetal facies'; thoracolumbar scoliosis, small hands, small penis (stretched penile length 1 cm), retractile testes; X-ray large cranium, crowded right sided ribs, absent left ribs 3 and 4, marked thoracic scoliosis to the right, lumbar scoliosis to the left, thoracic and lumbar hemivertebrae, short radius, short ulna; upper limb mesomelia more severe than lower limb; USG normal, ECG normal achondroplasia (prenatal) RRS1 Familial, autosomal recessive 02y06m - - short stature, facial dysmorphism - Johan den Dunnen 00406598
0000338929 - - - Isolated (sporadic) - - - - - Dan Feng Fang 00449784
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