Phenotypes for disease #04615 (MCCRP2 (microcephaly and chorioretinopathy, autosomal recessive, type 2 (MCCRP-2)), OMIM:616171)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000053267 - - - Unknown - - - - - Makiko Tsutsumi 00072170
0000061487 Intellectual disability, severe (HP:0010864) Absent speech (HP:0001344) Sloping forehead (HP:0000340) Prominent metopic ridge (HP:0005487) Upslanted palpebral fissure (HP:0000582) Blepharophimosis (HP:0000581) Epicanthus (HP:0000286) Macrotia (HP:0000400) Prominent nose (HP:0000448) Thin upper lip vermilion (HP:0000219) High arched palate (HP:0002705) Micrognathia (HP:0000347) Clinodactyly of the 5th finger (HP:0004209) Delayed skeletal maturation (HP:0002750) Hypoplasia of the radius (HP:0002984) Epiphysiolysis in distal femur (HP:0006461) Microcephaly (HP:0000252) Cortical gyral simplification (HP:0009879) - - Familial, autosomal recessive - 00y09m 00y09m? 9m - Bayram Toraman 00081828
0000061488 Intellectual disability, severe (HP:0010864) Sloping forehead (HP:0000340) Upslanted palpebral fissure (HP:0000582) Blepharophimosis (HP:0000581) Epicanthus (HP:0000286) Prominent nose (HP:0000448) Micrognathia (HP:0000347) - - Familial, autosomal recessive - - - - - Bayram Toraman 00081843
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