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

Official abbreviation MCCRP2
Name microcephaly and chorioretinopathy, autosomal recessive, type 2 (MCCRP-2)
OMIM ID 616171
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 3
Associated with 1 gene PLK4
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00072170 - - - F no Japan - - - - - MCCRP2 - PLK4 PLK4 2 1 Makiko Tsutsumi
00081828 FamPatVIII2 7-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents/relatives - F - - - - - - - MCCRP2 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) PLK4 PLK4 1 3 Bayram Toraman
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