Phenotypes for disease #01981 (OMOD (omodysplasia (OMOD)))

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000237130 see paper; ..., height 10th pecentile; short humeri; radial dislocation, limitation of movement; no vertebral anomalies; round face; frontal bossing, prominent forehead; no  small nose with broad tip; long philtrum; flat nasal bridge; cleft lip and cleft palate; hypoplastic genitalia/other genital anomalies; uterine anomalies omodysplasia OMOD2 Familial, autosomal dominant - - - - - Johan den Dunnen 00311882
0000237131 see paper; ..., height <5th pecentile; short humeri; radial dislocation, limitation of movement; short ulnae; short first metacarpal; femoral anomalies, proximal; short fibulae; vertebral anomalies; round face; frontal bossing, prominent forehead; small nose with broad tip; long philtrum; flat nasal bridge; no  cleft lip and cleft palate; no ypoplastic genitalia/other genital anomalies omodysplasia OMOD2 Familial, autosomal dominant - - - - - Johan den Dunnen 00311883
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