Phenotypes for disease #05170 (IE (encephalopathy, infantile (IE)))

8 entries on 1 page. Showing entries 1 - 8.
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Phenotype details     

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Diagnosis/Definite     

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Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000051396 Autosomal-Recessive Severe Infantile Encephalopathy; borderline cachexia (HP:0004326), progressive muscular hypotonia (HP:0001252), no microcephaly (-HP:0000252), no seizure (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) - - Familial, autosomal recessive 04y - - - - Pieter Klap 00065262
0000051397 Autosomal-Recessive Severe Infantile Encephalopathy; borderline cachexia (HP:0004326), progressive muscular hypotonia (HP:0001252), no microcephaly (-HP:0000252), single seizure (HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) - - Familial, autosomal recessive 08y - - - - Pieter Klap 00065260
0000051398 Autosomal-Recessive Severe Infantile Encephalopathy; Cachexia (HP:0004326), progressive muscular hypotonia (HP:0001252), Microcephaly (HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) - - Familial, autosomal recessive 07y 5.5m - - - Pieter Klap 00065259
0000051399 Autosomal-Recessive Severe Infantile Encephalopathy; Cachexia (HP:0004326), severe muscular hypotonia (HP:0001252), no microcephaly (-HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) - - Familial, autosomal recessive - 01y - - - Pieter Klap 00065258
0000051400 Autosomal-Recessive Severe Infantile Encephalopathy; cachexia (HP:0004326), severe muscular hypotonia (HP:0001252), Microcephaly (HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) - - Familial, autosomal recessive 02y - - - - Pieter Klap 00065257
0000051401 Autosomal-Recessive Severe Infantile Encephalopathy; cachexia (HP:0004326), severe muscular hypotonia (HP:0001252), microcephaly (HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) - - Familial, autosomal recessive 06y06m - - - - Pieter Klap 00065256
0000155130 fatal infantile encephalopathy - - Familial, autosomal recessive - - - - - Eric Shoubridge 00207359
0000155276 Systemic cyanosis and muscular hypotonia. Facial dysmorphism (depressed nasal bridge, large mouth, high-arched palate, micrognathia). Severe global DD, axial hypotonia and dyskinasia. Epileptic spasms and erratic myoclonic seizures. Progressive brain atrophy, delayed myelination, thin corpus callosum. Bilateral hydronephrosis. Elevated ALP level (405 IU/L) - - Familial, X-linked - 00y03m - - - Philippe Campeau 00207498
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