http://caligraph.org/ontology/Genetic_disorder_with_no_OMIM

CaLiGraph

Property	Value
rdf:type	owl:Class
rdfs:label	Genetic disorder with no OMIM
rdfs:subClassOf	Genetic disease or disorder
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Genetic_disorders_with_no_OMIM
is rdf:type of	Cooks syndrome Bare lymphocyte syndrome type II Tetrasomy 18p Congenital dyserythropoietic anemia Scott syndrome Monostotic fibrous dysplasia Bhaskar–Jagannathan syndrome Cerebellar hypoplasia Amelanism Ayazi syndrome Tetrasomy 9p Nullisomic Axanthism Leucism Hereditary spastic paraplegia Microorchidism Partial monosomy 13q Fibular hemimelia Aniridia renal agenesis psychomotor retardation Chromosome 15q partial deletion Isodicentric 15 Central nervous system cavernous hemangioma Erondu–Cymet syndrome Congenital fibrosis of the extraocular muscles Ring chromosome 20 syndrome Xanthochromism Pattern hair loss Fibrous dysplasia of bone Congenital dyserythropoietic anemia type I Hemimelia Ring chromosome 14 syndrome Hemoglobin variants Whiteface Congenital dyserythropoietic anemia type III Crouzonodermoskeletal syndrome Banti's syndrome Distal trisomy 10q Dentinogenesis imperfecta Erythrism Melanism Frontotemporal dementia and parkinsonism linked to chromosome 17 Snatiation Congenital dyserythropoietic anemia type II Benjamin syndrome Congenital dyserythropoietic anemia type IV 8p23.1 duplication syndrome GMS syndrome Lachiewicz–Sibley syndrome 2q37 deletion syndrome Singleton Merten syndrome Chromosome 15q trisomy Lethal white syndrome Lethal arthrogryposis with anterior horn cell disease Acytosiosis Zamzam–Sheriff–Phillips syndrome

About: clgo:Genetic_disorder_with_no_OMIM