Phenotypes for disease #05392 (CPCMR (cleft palate, cardiac defects, and mental retardation (CPCMR)), OMIM:600987)

11 entries on 1 page. Showing entries 1 - 11.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000125481 - MEIS2-related syndrome cleft palate (HP:0000175); prominent metopic ridge (HP:HP:0005487); downslanting palpebral fissures (HP:0000494); eversion of lower eyelids (HP:0007655); arched eyebrows (HP:0002553); hypoplastic alae nasi (HP:0000430); intellectual disability, mild (HP:0001256); perimembranous ventricular septal defect (HP:0011682); microcephaly (HP:0000252) Familial, autosomal dominant 05y - - - Jeroen Breckpot 00152012
0000125482 - MEIS2-related syndrome unilateral ptosis (HP:0007687); dysplastic ears (HP:0000377); intellectual disability, mild to moderate (HP:0001256); cleft palate (HP:0000175); autism (HP:0000717) Familial, autosomal dominant - - - - Jeroen Breckpot 00152013
0000125483 - MEIS2-related syndrome submucous cleft palate (HP:0011819); prominent metopic ridge (HP:0005487); protruding ears (HP:0000411); epicanthic folds (HP:0000286); hypoplastic alae nasi (HP:0000430); prominent ears (HP:0000411); frontal upsweep of hair (HP:0002236); intellectual disability, moderate (HP:0002342) Familial, autosomal dominant 04y - - - Jeroen Breckpot 00152014
0000125484 - MEIS2-related syndrome cleft palate (HP:0000175); mitral regurgitation (HP:0001653); broad forehead (HP:0000337); bitemporal narrowing (HP:0000341) Familial, autosomal dominant - - - - Jeroen Breckpot 00152015
0000125485 - MEIS2-related syndrome bifid uvula (HP:0000193); broad forehead (HP:0000337); medial flaring of eyebrows (HP:0010747); hypertelorism (HP:0000316); distichiasis (HP:0009743); thin upper lip (HP:0000219); beaked nose (HP:0003683); retrognathia (HP:0000278); intellectual disability, mild (HP:0001256); cryptorchidism (HP:0000028); iris nevus (HP:0011525); precocious puberty (HP:0008185); scoliosis (HP:0002650) Familial, autosomal dominant - - - - Jeroen Breckpot 00152123
0000125486 - MEIS2-related syndrome cleft palate (HP:0000175); high arched eyebrows (HP:0002553); thin eyebrows (HP:0045074); hypoplastic alae nasi (HP:0000430); short stature (HP:0004322); intellectual disability, mild (HP:0001256); hypoplastic corpus callosum (HP:0007370) Familial, autosomal dominant - - - - Jeroen Breckpot 00152124
0000125487 - MEIS2-related syndrome Tetralogy of Fallot (HP:0001636); Ebstein's malformation (HP:0010316); feeding difficulties (HP:0011968); strabismus (HP:0025068); scoliosis (HP:0002650); learning problems (HP:0001328) Familial, autosomal dominant 18y03m - - - Jeroen Breckpot 00152125
0000125488 - - cleft soft palate (HP:0000185); Ebstein's malformation (HP:0010316); VSD (HP:0011682); type secundum atrial septal defect (HP:0001684); high forehead (HP:0000348); broad forehead (HP:0000337); arched eyebrows (HP:0002553); thin eyebrows (HP:0045074); hypoplastic alae nasi (HP:0000430); short philtrum (HP:0000322); lowset ears (HP:0000369); dysplastic ears (HP:0000377); preauricular pit (HP:0004467); intellectual disability (HP:0001256); feeding difficulties (HP:0011968); oligodontia (HP:0000677); overriding toes (HP:0001845) Familial, autosomal dominant - - - - Jeroen Breckpot 00152126
0000125489 - MEIS2-related syndrome ventricular septal defect (HP:0011682); secundum atrial septal defect (HP:0001684); pulmonary vein stenosis (HP:0005304); frontal bossing (HP:0002007); high frontal hairline (HP:0009890); bitemporal narrowing (HP:0000341); short palpebral fissures (HP:0012745); hypertelorism (HP:0000316); full cheeks (HP:0000293); low nasal bridge (HP:0005280); anteverted nares (HP:0000463); small mouth (HP:0000160); microcephaly (HP:0000252); short stature (HP:0004322); intellectual disability, profound (HP:0002187); duodenal stenosis (HP:0100867); feeding difficulties (HP:0011968); hypothyroidism (HP:0000851); inguinal hernia (HP:0000023) Familial, autosomal dominant - - - - Jeroen Breckpot 00152128
0000308328 1y - Ventricular septal defect, Hypotonia, Motor delay, Expressive language delay, Pes planus, Gait ataxia, Neurodevelopmental abnormality, Impaired social interactions, Sleep disturbance, Delayed speech and language development, Genu valgum, Short stature Isolated (sporadic) - - - - Andreas Laner 00416608
0000324078 - - developmental delay, soft cleft palate, ventricular septal defect Isolated (sporadic) - - - - Marketa Wayhelova 00433655
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.