Poor head control

Symptom Information:

Symptom ID: HPO:0002421
Synonyms:
Poor head control [OMIM:Poor head control]
Quality:
Cross references:
OMIM: "Poor head control" [OMIM:Poor head control]
Is a (Direct Parents):
HPO         Muscle weakness
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:
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)