Phenotypes for disease #05224 (COMMAD (COMMAD syndrome (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness)), OMIM:617306)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Owner     

Individual ID     
0000078537 see paper; ..., colobomatous microphthalmia, microcornea with pannus, dense bilateral cataracts, translucent irides, profound congenital sensorineural hearing loss, lack visible pigment hair/skin/eyes, microphthalmia on prenatal ultrasound, macrocephaly - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100317
0000078540 see paper; ..., born with severe microphthalmia, profound congenital sensorineural hearing loss, lack of pigment hair/skin/eyes; relative macrocephaly, short stature, low weight - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100320
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