Phenotypes for disease #01705 (CMT4A (Charcot-Marie-Tooth disease, type 4A (CMT-4A)), OMIM:214400)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000081605 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103674
0000081606 Charcot-Marie-Tooth disease 4A, early onset axonal - - Unknown - - - - - Johan den Dunnen 00103675
0000081608 Charcot-Marie-Tooth disease 4A, early onset axonal - - Unknown - - - - - Johan den Dunnen 00103677
0000081612 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103681
0000081615 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103684
0000081616 Charcot-Marie-Tooth disease 4A - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103685
0000081621 Charcot-Marie-Tooth disease 4A - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103690
0000081622 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103691
0000081624 Charcot-Marie-Tooth disease 4A, early onset axonal - - Unknown - - - - - Johan den Dunnen 00103693
0000081634 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103703
0000081635 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103704
0000081636 Charcot-Marie-Tooth disease 4A - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103705
0000081641 Charcot-Marie-Tooth disease 4A - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103710
0000081644 Charcot-Marie-Tooth disease 4A, early onset axonal - - Unknown - - - - - Johan den Dunnen 00103713
0000081647 Charcot-Marie-Tooth disease 4A - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103716
0000081649 Charcot-Marie-Tooth disease 4A, early onset axonal - - Unknown - - - - - Johan den Dunnen 00103718
0000081652 Charcot-Marie-Tooth disease 4A - - Unknown - - - - - Johan den Dunnen 00103721
0000081656 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103723
0000081657 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103724
0000081658 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00103725
0000292069 Gait disturbance (HP:0001288),Lower limb amyotrophy (HP:0007210), Split hand (HP:0001171), Difficulty running (HP:0009046), Difficult climbing stairs (HP:0003551), Lower limb muscle weakness (HP:0007340), High-arched feet Pes cavus (HP:0001761), Ankle weakness (HP:0031374), Limited ankle dorsiflexion (HP:0033526), No spinal deformities (-HP:0008443), Reduced tendon reflexes (HP:0001315), No impaired tactile sensation (-HP:0010830), No impaired pain sensation (-HP:0007328), Decreased nerve conduction velocity (HP:0000762) CMT CMT4A Familial, autosomal recessive 16y - 06y Difficulty running (HP:0009046), Difficult climbing stairs (HP:0003551) - Yvet den Hartog 00398980
0000292212 Lower limb amyotrophy (HP:0007210), Upper limb amyotrophy (HP:0009129), Intrinsic hand muscle atrophy (HP:0008954), Areflexia (HP:0001284), Proximal muscle weakness (HP:0003701), Somatic sensory dysfunction (HP:0003474), Impaired distal tactile sensation (HP:0006937), Impaired pain sensation (HP:0007328), Pes cavus (HP:0001761), No hoarse voice (-HP:0001609), No vocal cord paresis (-HP:0001604), No diaphragmatic paralysis (HP:0006597), No cognitive impairment (-HP:0100543), No Decreased compound muscle action potential amplitude (-HP:0033383), No respiratory failure (-HP:0002878), Difficulty running (HP:0009046) CMT CMT4A Familial, autosomal recessive 16y - 02y03m Difficulty running (HP:0009046) - Yvet den Hartog 00398982
0000292213 Lower limb amyotrophy (HP:0007210), Upper limb amyotrophy (HP:0009129), Intrinsic hand muscle atrophy (HP:0008954), Areflexia (HP:0001284), Proximal muscle weakness (HP:0003701), Somatic sensory dysfunction (HP:0003474), Impaired distal tactile sensation (HP:0006937), Impaired pain sensation (HP:0007328), Pes cavus (HP:0001761), No hoarse voice (-HP:0001609), No vocal cord paresis (-HP:0001604), No diaphragmatic paralysis (HP:0006597), No cognitive impairment (-HP:0100543), No Decreased compound muscle action potential amplitude (-HP:0033383), No respiratory failure (-HP:0002878), Difficulty running (HP:0009046) CMT CMT4A Familial, autosomal recessive 12y - 02y03m Difficulty running (HP:0009046) - Yvet den Hartog 00399124
0000292214 Upper limb amyotrophy (HP:0009129), Intrinsic hand muscle atrophy (HP:0008954), Areflexia (HP:0001284), Proximal muscle weakness (HP:0003701), Somatic sensory dysfunction (HP:0003474), Impaired distal tactile sensation (HP:0006937), Impaired pain sensation (HP:0007328), No hoarse voice (-HP:0001609), No vocal cord paresis (-HP:0001604), No diaphragmatic paralysis (HP:0006597), No cognitive impairment (-HP:0100543), No Decreased compound muscle action potential amplitude (-HP:0033383), No respiratory failure (-HP:0002878), Difficulty running (HP:0009046) CMT CMT4A Familial, autosomal recessive 03y04m - 02y03m Difficulty running (HP:0009046) - Yvet den Hartog 00399125
0000293261 Skeletal muscle atrophy (HP:0003202), Abnormal bone ossification (HP:0011849), No abnormal bone structure (-HP:0003330), Ankle flexion contracture (HP:0006466), Pes cavus (HP:0001761), Muscle weakness (HP:0001324), Bilateral talipes equinovarus (HP:0001776), Abnormality of the wrist (HP:0003019), Joint contracture of the hand (HP:0009473), Contracture involving the joints of the feet (HP:0008366), No poor speech (-HP:0002465), No hearing abnormality (-HP:0000364), No abnormality of vision (-HP:0000504), No intellectual disability (-HP:0001249), Poor gross motor coordination (HP:0007015), Somatic sensory dysfunction (HP:0003474), Peripheral neuropathy (HP:0009830), Reduced bone mineral density (HP:0004349), No skeletal dysplasia (HP:0002652), Gait disturbance (HP:0001288) CMT CMT4A Familial, autosomal recessive 29y - 05y Gait disturbance (HP:0001288) - Yvet den Hartog 00400221
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