Phenotypes for disease #05031 (CATMANS (Catel-Manzke syndrome (CATMANS)), OMIM:616145)

4 entries on 1 page. Showing entries 1 - 4.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000230290 short stature (HP:0004322) -2.3 SD; vertebral anomalies (HP:0003468), butterfly vertebrae T10–11, scoliosis; no talipes (-HP:0001883); Manzke dysostosis/finger hyperphalangism (HP:0009495/HP:0030367); no other limb defects (-HP:0040068); no Pierre Robin sequence with cleft palate (-HP:0000201); microretrognathia (HP:0000308); no renal malformation (-HP:0012210); congenital heart defect (HP:0001627), hypoplastic left heart; mild developmental delay (HP 0001263); no muscular hypotonia (-HP:0001252); no failure to thrive (-HP:0001531); no microcephaly (-HP:0000252); facial dysmorphism (HP:0001999); no joint hypermobility (-HP:0001382); hepatomegaly Catel-Manzke syndrome - Familial, autosomal recessive 13y - - - - Johan den Dunnen 00303206
0000230291 short stature (HP:0004322) -4.6 SD; vertebral anomalies (HP:0003468), butterfly vertebra T8; no talipes (-HP:0001883); Manzke dysostosis/finger hyperphalangism (HP:0009495/HP:0030367); other limb defects (HP:0040068), long thumbs; no Pierre Robin sequence with cleft palate (-HP:0000201); no microretrognathia (-HP:0000308); no renal malformation (-HP:0012210); congenital heart defect (HP:0001627), Tetralogy of Fallot, anomalous origin left coronary artery from pulmonary artery; developmental delay (HP 0001263); severe muscular hypotonia (HP:0001252); failure to thrive (HP:0001531), PEG feeding; microcephaly (HP:0000252) -6.4 SD; facial dysmorphism (HP:0001999); no joint hypermobility (-HP:0001382); sensorineural hearing loss (HP:0000407); malformation of cochlea and semicircular canals (HP:0008554, HP:0011380); bilateral single transverse palmar crease Catel-Manzke syndrome - Familial, autosomal recessive 3y - - - - Johan den Dunnen 00303207
0000230292 short stature (HP:0004322) -2.2 SD; no vertebral anomalies (-HP:0003468); no talipes (-HP:0001883); Manzke dysostosis/finger hyperphalangism (HP:0009495/HP:0030367); other limb defects (HP:0040068), short 3rd fingers and short 2nd metacarpals due to accessory ossicles, clinodactyly of 5th fingers, 2,3-toe syndactyly; no Pierre Robin sequence with cleft palate (-HP:0000201); microretrognathia (HP:0000308); renal malformation (HP:0012210), unilateral renal agenesis; congenital heart defect (HP:0001627), secundum atrial septal defect, subaortic ventricular septal defect; mild developmental delay (HP 0001263); no muscular hypotonia (-HP:0001252); no failure to thrive (-HP:0001531); microcephaly (HP:0000252) -2.3 SD; facial dysmorphism (HP:0001999); joint hypermobility (HP:0001382) Catel-Manzke syndrome - Familial, autosomal recessive 5y - - - - Johan den Dunnen 00303208
0000254693 - Catel-Manzke like syndrome, Manzke dysostosis, hyperphalangism - Unknown - - - - - Cynthia Silveira 00359452
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