Phenotypes for disease #05169 (MGORS (Meier-Gorlin syndrome (MGORS)))

6 entries on 1 page. Showing entries 1 - 6.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000051395 short stature (HP:0004322), microtia (HP:0008551), patella aplasia (HP:0006443), low birth weight (HP:0001518), low weight (HP:0004325), reduced head circumference (HP:0000252), delayed bone age (HP:0002750), frontal bossing (HP:?) or high forehead (HP:0000348), down-slanted palpebral fissures (HP:0000494), posteriorly rotated ears (HP:0000358), upturned nose (HP:0000463), hypoplastic nares (HP:0000430), full lips (HP:0012471), micro-/retrognathia (HP:0000308), no motor delay (-HP:0001270), no speech delay (-HP:0000750), no pulmonary emphysema (-HP:0002097), laryngomalacia (HP:0001601), tracheo-/bronchomalacia (HP:0002786), feeding problems in infancy (HP:0011968), failure to thrive (HP:0001508), gastresophageal reflux (HP:0002020), abnormal genitalia (HP:0010460), hypoplastic labia majora (HP:0000059), trichiasis (HP:0001128), nanophthalmos (HP:0000568) - - Familial, autosomal dominant 00y34m - - - - Jamie Zeegers 00065288
0000051410 short stature (HP:0004322), microtia (HP:0008551), patella aplasia (HP:0006443), low birth weight (HP:0001518), reduced birth lengt (HP:?), birth head circumference (HP:0011451), low weight (HP:0004325), delayed bone age (HP:0002750), frontal bossing (HP:?) or high forehead (HP:0000348), no down-slanted palpebral fissures (-HP:0000494), no posteriorly rotated ears (-HP:0000358), no upturned nose (-HP:0000463), hypoplastic nares (HP:0000430), full lips (HP:0012471), micro-/retrognathia (HP:0000308), motor delay (HP:0001270), speech delay (HP:0000750), developmental assessment (HP:?), pulmonary emphysema (HP:0002097), no laryngomalacia (-HP:0001601), no tracheo-/bronchomalacia (-HP:0002786), feeding problems in infancy (HP:0011968), failure to thrive (HP:0001508), no gastresophageal reflux (-HP:0002020), no abnormal genitalia (-HP:0010460), hypospadias (HP:0000047), cryptorchidism (HP:0000028), no rIncreased/marked lumbar lordosis (HP:0002938) Urethral stenosis/ dysplasia (HP:0008661)enal anomalies (-HP:0000077), - - Familial, autosomal dominant 17y 00y04m - - - Jamie Zeegers 00065295
0000051412 short stature (HP:0004322), microtia (HP:0008551), patella aplasia (HP:0006443), reduced birth weight (HP:0001518), reduced birth lengt (HP:?), reduced weight (HP:0004325), reduced head circumference (HP:0000252), frontal bossing (HP:?) or high forehead (HP:0000348), no down-slanted palpebral fissures (-HP:0000494), posteriorly rotated ears (HP:0000358), no upturned nose (-HP:0000463), hypoplastic nares (HP:0000430), full lips (HP:0012471), micro-/retrognathia (HP:0000308), motor delay (HP:0001270), speech delay (HP:0000750), developmental assessment IQ= 59 at age 14 years (HP:?), no pulmonary emphysema (-HP:0002097), no laryngomalacia (-HP:0001601), no tracheo-/bronchomalacia (-HP:0002786), feeding problems in infancy (HP:0011968), no failure to thrive (-HP:0001508), no gastresophageal reflux (-HP:0002020), no renal anomalies (HP:0000077 ), Increased/marked lumbar lordosis (HP:0002938), bilateral congenital hip subluxation (HP:0030043), strabismus (HP:0000486), cleft palate (palatum molle) (HP:0000175) - - Familial, autosomal dominant 03y04m 03y - - - Jamie Zeegers 00065297
0000061473 - Growth parameters below the 3rd centile; no microcephaly. Normal Psychomotor development and brain NMR. - - Familial, autosomal recessive - - - - - Annalisa Vetro 00081271
0000243066 short stature microcephaly microtia bilateral absent patella absent breast development MGORS MGORS Familial, autosomal recessive - - - - - Louise Bicknell 00324523
0000243069 short stature microcephaly microtia congenital lobar emphysema myopia MGORS - Familial, autosomal recessive - - - - - Louise Bicknell 00324525
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