Poor head control
Symptom Information:
Symptom ID: | HPO:0002421 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Poor head control(HPO:0002421) MedDRA: |
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Database Frequency: | 23 / 7739 | ||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
CEDNIK syndrome | (Orphanet:66631) |
Classic multiminicore myopathy | (Orphanet:324604) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | (Orphanet:300179) |
GM2-gangliosidosis, AB variant | (Orphanet:309246) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Infantile hypophosphatasia | (Orphanet:247651) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C | (OMIM:615501) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 | (OMIM:615249) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 | (OMIM:615351) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
Pontocerebellar hypoplasia type 3 | (Orphanet:97249) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Rigid spine syndrome | (Orphanet:97244) |
Tay-Sachs disease | (Orphanet:845) |