Phenotypes for disease #05072 (WRWF (Wieacker-Wolff syndrome (WRWF)), OMIM:314580)

35 entries on 1 page. Showing entries 1 - 35.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000174438 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234016
0000174439 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234017
0000174440 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234018
0000174441 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234019
0000174442 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234020
0000174443 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234021
0000174444 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234022
0000174445 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234023
0000174446 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234024
0000174447 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234025
0000174448 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234026
0000174449 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234027
0000174450 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234028
0000174451 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234029
0000174452 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234030
0000174453 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234031
0000174454 - ZARD - Isolated (sporadic) - - - - - Vera Kalscheuer 00234032
0000174455 - ZARD - Familial, X-linked recessive - - - - - Vera Kalscheuer 00234033
0000174456 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234034
0000174457 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234035
0000174458 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234036
0000174459 - ZARD - Familial, X-linked dominant - - - - - Vera Kalscheuer 00234037
0000174460 - ZARD - Isolated (sporadic) - - - - - Vera Kalscheuer 00234038
0000174462 dwarfism (HP:0001516) (2); long (flat) philtrum (HP:0000299) (2); oral motor dysfunction (HP:0005216) (1); low-set ears (HP:0000369) (2); ptosis (HP:0001488) (3); upturned nares (HP:0000463) (2); high-arched palate (HP:0000218) (2); carp-shaped mouth (HP:0010806) (2); drooling (HP:0002307) (3); short neck (with limited rotation) (HP:0000470) (2); neonatal respiratory distress (HP:0002643) (3); humeroscapular mobility restriction (HP:0006467) (2); narrow shoulders or thorax (HP:0006664) (3); poor feeding (HP:0002022) (4); kyphosis, lordosis or scoliosis (HP:0002751) (3); congenital hip dislocations or hip flexion contractures (HP:0001374) (4); flexion contractures of elbows or knees (HP:0002987, HP:0002978) (3); proximally placed thumbs (HP:0009623) (2); camptodactyly (HP:0001215) (5); ulnar deviation finger (HP:0009465) (3); proximally placed toes (HP:0001780) (4); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (5); high anterior hairline (HP:0000294) (2); distal muscle weakness (HP:0002460) (2); edema or fat pads (hands and/or feet) (HP:0007514) (3); retardation of motor development (HP:0001263) (5); intellectual disability (HP:0001249) (5); spasticity (HP:0001257) (5); seizures (HP:0001250) (4); MRI delayed myelination (HP:0002188) (2); MRI diffuse cerebral atrophy (HP:0002283) (3) arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234040
0000174463 equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1) arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234041
0000174464 dwarfism (HP:0001516) (1); long (flat) philtrum (HP:0000299) (5); ptosis (HP:0001488) (1); upturned nares (HP:0000463) (5); broad alveolar ridges (HP:0000187) (5); high-arched palate (HP:0000218) (5); carp-shaped mouth (HP:0010806) (5); short neck (with limited rotation) (HP:0000470) (1); neonatal respiratory distress (HP:0002643) (5); humeroscapular mobility restriction (HP:0006467) (1); kyphosis, lordosis or scoliosis (HP:0002751) (1); congenital hip dislocations or hip flexion contractures (HP:0001374) (2); short limbs (HP:0009826) (2); flexion contractures of elbows or knees (HP:0002987, HP:0002978) (2); proximally placed thumbs (HP:0009623) (1); camptodactyly (HP:0001215) (2); ulnar deviation finger (HP:0009465) (1); proximally placed toes (HP:0001780) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (2); high anterior hairline (HP:0000294) (5); edema or fat pads (hands and/or feet) (HP:0007514) (1); retardation of motor development (HP:0001263) (1); intellectual disability (HP:0001249) (1); seizures (HP:0001250) (1); MRI delayed myelination (HP:0002188) (1) arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234042
0000174465 urine incontinence (HP:0000020) (1); distal muscle weakness (HP:0002460) (3); intellectual disability (HP:0001249) (3); dysarthria and/or deficit in expressive language (HP:0001260) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (3); camptodactyly (HP:0001215) (5) arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234043
0000174466 drooling (HP:0002307) (2); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (2); retardation of motor development (HP:0001263) (2); intellectual disability (HP:0001249) (2); spasticity (HP:0001257) (2); seizures (HP:0001250) (1); arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234044
0000174467 intellectual disability (HP:0001249) (1) arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234045
0000174469 intellectual disability (HP:0001249) (2) arthrogryposis multiplex congenita, intellectual disability WRWF Familial, X-linked recessive - - - - - Johan den Dunnen 00234047
0000174470 dwarfism (HP:0001516) (1); long (flat) philtrum (HP:0000299) (1); oral motor dysfunction (HP:0005216) (1); low-set ears (HP:0000369) (1); ptosis (HP:0001488) (1); upturned nares (HP:0000463) (1); broad alveolar ridges (HP:0000187) (1); high-arched palate (HP:0000218) (1); carp-shaped mouth (HP:0010806) (1); drooling (HP:0002307) (1); short neck (with limited rotation) (HP:0000470) (1); neonatal respiratory distress (HP:0002643) (1); humeroscapular mobility restriction (HP:0006467) (1); narrow shoulders or thorax (HP:0006664) (1); poor feeding (HP:0002022) (1); kyphosis, lordosis or scoliosis (HP:0002751) (1); congenital hip dislocations or hip flexion contractures (HP:0001374) (1); short limbs (HP:0009826) (1); flexion contractures of elbows or knees (HP:0002987, HP:0002978) (1); proximally placed thumbs (HP:0009623) (1); camptodactyly (HP:0001215) (1); ulnar deviation finger (HP:0009465) (1); proximally placed toes (HP:0001780) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1); high anterior hairline (HP:0000294) (1); distal muscle weakness (HP:0002460) (1); edema or fat pads (hands and/or feet) (HP:0007514) (1); retardation of motor development (HP:0001263) (1); intellectual disability (HP:0001249) (1); spasticity (HP:0001257) (1); seizures (HP:0001250) (1); MRI delayed myelination (HP:0002188) (1); MRI diffuse cerebral atrophy (HP:0002283) (1) arthrogryposis multiplex congenita, intellectual disability WRWF Isolated (sporadic) 03y10m - - - - Johan den Dunnen 00234048
0000174471 urine incontinence (HP:0000020) (1); distal muscle weakness (HP:0002460) (1); intellectual disability (HP:0001249) (1); dysarthria and/or deficit in expressive language (HP:0001260) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1); camptodactyly (HP:0001215) (1) arthrogryposis multiplex congenita, intellectual disability WRWF Isolated (sporadic) 9y - - - - Johan den Dunnen 00234049
0000174472 urine incontinence (HP:0000020) (1); distal muscle weakness (HP:0002460) (1); intellectual disability (HP:0001249) (1); dysarthria and/or deficit in expressive language (HP:0001260) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1); camptodactyly (HP:0001215) (1) arthrogryposis multiplex congenita, intellectual disability WRWF Isolated (sporadic) 13y - - - - Johan den Dunnen 00234050
0000231987 - - - Unknown - - - - - Sha Hong 00306143
0000308162 Global developmental delay, Expressive language delay, Hypotonia, Mild microcephaly - - Unknown - - - - - Andreas Laner 00416442
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